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Water Science and Technology : a... Apr 2021The rapid expansion of global trade and human activities has resulted in a massive increase in wastewater pollution into the atmosphere. Suspended solids, organic and...
The rapid expansion of global trade and human activities has resulted in a massive increase in wastewater pollution into the atmosphere. Suspended solids, organic and inorganic particles, dissolved solids, heavy metals, dyes, and other impurities contained in wastewater from various sources are toxic to the atmosphere and pose serious health risks to humans and animals. Coagulation-flocculation technology is commonly used in wastewater treatment to remove cell debris, colloids, and contaminants in a comfortable and effective manner. Flocculants, both organic and inorganic, have long been used in wastewater treatment. However, because of their low performance, non-biodegradability, and associated health risks, their use has been limited. The use of eco-friendly bioflocculants in wastewater treatment has become essential due to the health implications of chemical flocculants. Because of their availability, biodegradability, and protection, plant-derived coagulants/flocculants and plant-based grafted bioflocculants have recently made significant progress in wastewater treatment. This study will undoubtedly provide a clearer understanding of the current state, challenges, and solutions for bioflocculation in wastewater remediation using green materials for the sake of a cleaner climate.
Topics: Animals; Coloring Agents; Flocculation; Humans; Metals, Heavy; Waste Disposal, Fluid; Wastewater; Water Purification
PubMed: 33905353
DOI: 10.2166/wst.2021.100 -
Journal of Environmental Sciences... Nov 2020Few studies have been carried out to connect nutrient recovery as struvite from wastewater and sustainable utilization of the recovered struvite for copper and zinc...
Few studies have been carried out to connect nutrient recovery as struvite from wastewater and sustainable utilization of the recovered struvite for copper and zinc immobilization in contaminated soil. This study revealed the effect of struvite on Cu and Zn immobilization in contaminated bio-retention soil in the presence of commonly exuded plant organic acids. The research hypothesis was that the presence of both struvite and organic acids may influence the immobilization of Cu and Zn in soil. The outcome of this research confirmed that more than 99% of Cu and Zn was immobilized in bio-retention filter media by struvite application. Water-soluble Cu and Zn concentrations of struvite treated soil were less than 1.83 and 0.86 mg/kg respectively, and these concentrations were significantly lower compared to the total Cu and Zn content of 747.05 mg/kg in the contaminated soil. Application of struvite to Cu- and Zn-contaminated soil resulted in formation of compounds similar to zinc phosphate tetrahydrate (Zn(PO)•4HO) and amorphous Cu and Zn phases. Struvite was effective in heavy metal remediation in acidic soil regardless of the presence of Ca impurities in struvite and the presence of plant organic acids in soil. Overall, this study revealed that struvite recovered from wastewater treatment plants has potential for use as an amendment for heavy metal remediation in contaminated bio-retention soil.
Topics: Copper; Metals, Heavy; Soil; Soil Pollutants; Struvite; Zinc
PubMed: 32933738
DOI: 10.1016/j.jes.2020.04.023 -
Journal of the American Chemical Society Apr 2023Organic hierarchical branch micro/nanostructures constituted by single crystals with inherent multichannel characteristics exhibit superior potential in regulating...
Organic hierarchical branch micro/nanostructures constituted by single crystals with inherent multichannel characteristics exhibit superior potential in regulating photon transmission for photonic circuits. However, organic branch micro/nanostructures with precise branch positions are extremely difficult to achieve due to the randomness of the nucleation process. Herein, by taking advantage of the dislocation stress field-impurity interaction that solute molecules deposit preferentially along the dislocation line, twinning deformation was introduced into microcrystals to induce oriented nucleation sites, and ultimately organic branch microstructures with controllable branch sites were fabricated. The growth mechanism of these controllable single crystals with an angle of 140° between trunk and branch is attributed to the low lattice mismatching ratio (η) of 4.8%. These as-prepared hierarchical branch single crystals with asymmetrical optical waveguide characteristics have been demonstrated as an optical logic gate with multiple input/out channels, which provides a route to command the nucleation sites and offers potential applications in the organic optoelectronics at the micro/nanoscale.
PubMed: 37040147
DOI: 10.1021/jacs.3c02061 -
Nanomaterials (Basel, Switzerland) May 2023Photovoltaics are being transformed by perovskite solar cells. The power conversion efficiency of these solar cells has increased significantly, and even higher...
Photovoltaics are being transformed by perovskite solar cells. The power conversion efficiency of these solar cells has increased significantly, and even higher efficiencies are possible. The scientific community has gained much attention due to perovskites' potential. Herein, the electron-only devices were prepared by spin-coating and introducing the organic molecule dibenzo-18-crown-6 (DC) to CsPbIBr perovskite precursor solution. The current-voltage (I-V) and J-V curves were measured. The morphologies and elemental composition information of the samples were obtained by SEM, XRD, XPS, Raman, and photoluminescence (PL) spectroscopies. The distinct impact of organic DC molecules on the phase, morphology, and optical properties of perovskite films are examined and interpreted with experimental results. The efficiency of the photovoltaic device in the control group is 9.76%, and the device efficiency gradually increases with the increase of DC concentration. When the concentration is 0.3%, the device efficiency is the best, reaching 11.57%, short-circuit current is 14.01 mA/cm, the open circuit voltage is 1.19 V, and the fill factor is 0.7. The presence of DC molecules effectively controlled the perovskite crystallization process by inhibiting the in-situ generations of impurity phases and minimizing the defect density of the film.
PubMed: 37299654
DOI: 10.3390/nano13111751 -
Chemical Society Reviews Jun 2024Seawater electrolysis for the production of fuels and chemicals involved in onshore and offshore plants powered by renewable energies offers a promising avenue and... (Review)
Review
Seawater electrolysis for the production of fuels and chemicals involved in onshore and offshore plants powered by renewable energies offers a promising avenue and unique advantages for energy and environmental sustainability. Nevertheless, seawater electrolysis presents long-term challenges and issues, such as complex composition, potential side reactions, deposition of and poisoning by microorganisms and metal ions, as well as corrosion, thus hindering the rapid development of seawater electrolysis technology. This review focuses on the production of value-added fuels (hydrogen and beyond) and fine chemicals through seawater electrolysis, as a promising step towards sustainable energy development and carbon neutrality. The principle of seawater electrolysis and related challenges are first introduced, and the redox reaction mechanisms of fuels and chemicals are summarized. Strategies for operating anodes and cathodes including the development and application of chloride- and impurity-resistant electrocatalysts/membranes are reviewed. We comprehensively summarize the production of fuels and chemicals (hydrogen, carbon monoxide, sulfur, ammonia, ) at the cathode and anode seawater electrolysis, and propose other potential strategies for co-producing fine chemicals, even sophisticated and electronic chemicals. Seawater electrolysis can drive the oxidation and upgrading of industrial pollutants or natural organics into value-added chemicals or degrade them into harmless substances, which would be meaningful for environmental protection. Finally, the perspective and prospects are outlined to address the challenges and expand the application of seawater electrolysis.
PubMed: 38855878
DOI: 10.1039/d3cs00822c -
Scientific Reports Nov 2023A robust, stability-indicating, and eco-friendly proton nuclear magnetic resonance (H-qNMR) method was developed for the concurrent determination of three...
Utility and greenness appraisal of nuclear magnetic resonance for sustainable simultaneous determination of three 1,4-benzodiazepines and their main impurity 2-amino-5-chlorobenzophenone.
A robust, stability-indicating, and eco-friendly proton nuclear magnetic resonance (H-qNMR) method was developed for the concurrent determination of three 1,4-benzodiazepines (BDZs), namely diazepam (DZP), alprazolam (ALP), and chlordiazepoxide (CDP) and their common impurity, synthesis precursor, and degradation product; 2-amino-5-chlorobenzophenone (ACB). In the present method, a novel approach was developed for composing a green and cost-efficient solvent system as an alternative to the common NMR organic solvents utilizing 0.3 M sodium dodecyl sulfate prepared in deuterated water. The conducted method is characterized by simplicity with no need for sample pretreatment or labeling. Phloroglucinol was used as an internal standard. The chosen signals for the determinations of ALP, CDP, DZP and ACB were at 2.35 ppm (singlet), 2.84 ppm (singlet), 3.11 ppm (singlet), and 6.90 ppm (doublet of doublet), respectively. The proposed method possessed linearity over the concentration range of 0.25-15.0 mg ml for DZP, ALP, CDP and of 0.5-25.0 mg ml for ACB with LOD values of 0.06, 0.03, 0.07 and 0.16 mg ml respectively, and LOQ values of 0.18, 0.09, 0.21 and 0.49 mg ml, respectively. Accuracy of the method was evidenced by excellent recovery% (99.57-99.90%) and small standard deviation (≥ 1.10) for the three analyzed drugs. Intra- and inter-day precision were determined with coefficient of variation ranging from 0.12 to 1.14 and from 0.72 to 1.67, respectively. For the studied compounds, appraisal of the method greenness was achieved via four approaches: Analytical Eco-Scale, Green Analytical Procedure Index (GAPI), Analytical greenness metric (AGREE), and RGB Additive Color Model. The results proved that the proposed method has the privilege of being a green analytical method.
Topics: Benzodiazepines; Benzophenones; Diazepam; Magnetic Resonance Spectroscopy; Solvents
PubMed: 38036558
DOI: 10.1038/s41598-023-48416-7 -
Se Pu = Chinese Journal of... Apr 2021Istradefylline is a novel selective adenosine A receptor antagonist that is used to treat Parkinson's disease and improve motor dysfunction in the early stage of this...
Istradefylline is a novel selective adenosine A receptor antagonist that is used to treat Parkinson's disease and improve motor dysfunction in the early stage of this disease. During the synthesis of intermediate A1 (6-amino-1,3-diethyl-2,4-(1,3)-pyrimidinedione), at least two by-products were formed under alkaline or high-temperature conditions. In a previous study, one of the by-products in the synthesis of the intermediate was studied, and its structure was identified as ()-ethyl-2-cyano-3-ethylamino-2-butene amide. In this study, we used high performance liquid chromatography (HPLC) to analyze another impurity formed during the synthesis of A1, and the following steps were executed: 0.4 g of intermediate was weighed and added to a 50 mL beaker, followed by the sequential addition of 8 mL water and 8 mL acetonitrile, and then, ultrasonic dissolution was performed. Finally, the solution was filtered through a 0.45-μm organic membrane and the test sample solution was obtained. We used the Agilent zorbax C18 chromatography column, with acetonitrile (A)/water(B) as the mobile phase under gradient elution ((/A∶B)=/20∶80, /60∶40, -/90∶10). The detector wavelength is 268 nm. In order to separate the impurity from A1, we used a Ceres B preparative column, with acetonitrile-water (30/70, v/v) as the mobile phase. The flow rate was set at 30 mL/min, and the detection wavelength was 268 nm. The structure of the impurity was confirmed by high-resolution mass spectrometry (HRMS), one-dimensional nuclear magnetic resonance (NMR), and two-dimensional nuclear magnetic resonance (2D NMR), and characterized by single-crystal X-ray diffraction (XRD). In MS experiments, an electrospray ionization (ESI) source was used with positive ion scanning. In the NMR experiments, we used tetramethylsilane (TMS) as the internal standard and deuterated dimethyl sulfoxide (DMSO-d) as the solvent to obtain the spectra. The results of preparative high performance liquid chromatography (Prep-HPLC) showed that good separation effect could be achieved by isocratic elution, and the impurity was perfectly separated. TheH-NMR spectral data are as follows:H-NMR (600 MHz, DMSO): 1.01 (q, =6.9 Hz, 3H), 1.02 (q, =6.9 Hz, 3H), 1.07 (t, =6.9 Hz, 3H), 3.04 (p, =6.8 Hz, 2H), 3.74 (q, =7.0 Hz, 2H), 3.94 (q, =7.1 Hz, 2H), 5.85 (s, 1H). The C-NMR spectral data are summarized as follows: C-NMR (150 MHz, DMSO): 13.9, 14.1, 15.9, 34.6, 34.9, 36.9, 81.9, 152.2, 153.3, 159.3, 162.0. The impurity was characterized by single-crystal XRD, and its spatial structure was further verified and determined as 1-(1,3-diethyl-2,6-dioxo-1,2,3,6-tetrahydropyrimidin-4-yl)-3-ethylurea. Based on the chemical structure of the impurity, we propose the following mechanism for the impurity: when A1 is synthesized under alkaline conditions or at high temperature, excessive diethylurea continues to undergo amidation with A1 to obtain this by-product. Although the formation mechanism of the impurity studied in this paper is different from that of the intermediate A1 impurity ()-ethyl-2-cyano-3-ethylamino-2-butene amide, both the impurities are formed at high temperatures. Both will be accompanied by A1 in the subsequent reaction of istradefylline synthesis. The relationship between drug impurities and drug safety is a complex relationship that is affected by many factors. Generally, most impurities in drugs have potential biological activities, and some even interact with the drugs, thus affecting their efficacy and safety and inducing toxic effects. Therefore, to ensure the quality of istradefylline, it is necessary to control the impurity content during the production. The findings of this paper may provide guidelines for controlling the impurity content in istradefylline.
Topics: Chromatography, High Pressure Liquid; Drug Contamination; Mass Spectrometry; Purines
PubMed: 34227764
DOI: 10.3724/SP.J.1123.2020.10013 -
ACS Applied Materials & Interfaces Oct 2020High-entropy oxides (HEOs) have attracted increasing interest owing to their unique structures and fascinating physicochemical properties. Spherical mesoporous HEOs...
High-entropy oxides (HEOs) have attracted increasing interest owing to their unique structures and fascinating physicochemical properties. Spherical mesoporous HEOs further inherit the advantages of spherical mesoporous materials including high surface area and tunable pore size. However, it is still a huge challenge to construct HEOs with uniform spheres and a mesoporous framework. Herein, a wet-chemistry sol-gel strategy is demonstrated for the synthesis of spherical mesoporous HEOs (e.g., Ni-Co-Cr-Fe-Mn oxide) with high specific surface area (42-143 m/g), large pore size (5.5-8.3 nm), unique spherical morphology (∼55 nm), and spinel structure without any impure crystal phase using polyphenol as a polymerizable ligand. The metal/polyphenol-formaldehyde resin colloidal spheres are first synthesized via a sol-gel process. Because of their abundant catechol groups and strong chelating ability with different metal species, polyphenols can not only accommodate five different metal ions in their networks but also be well polymerized by formaldehyde to form colloidal spheres. After calcination, the metal species aggregate together to form HEOs, while the organic resin is fully decomposed to produce mesopores. Because of the open framework with accessible mesopores, they could be used as a peroxymonosulfate catalyst for degradation of organic pollutants and a nanoplatform for efficient detection of DNA. This work demonstrates a straightforward sol-gel strategy for design and synthesis of spherical mesoporous high-entropy materials, which would promote the exploration of new properties of high-entropy materials and extend their application.
PubMed: 32915530
DOI: 10.1021/acsami.0c11899 -
Physical Chemistry Chemical Physics :... Oct 2023The power conversion efficiencies of organic solar cells (OSCs) have been greatly improved in recent years. However, latest experimental data of high efficiency OSCs,...
The power conversion efficiencies of organic solar cells (OSCs) have been greatly improved in recent years. However, latest experimental data of high efficiency OSCs, the sublinear relationship between the short circuit current density () and light intensity (), and the effects of energetic disorder in bulk heterojunction organic solar cells have not been understood. An analytical model for high-efficiency OSCs is proposed, which takes most physical factors into account that have been ignored in most previous models, including practical solar spectra and absorption spectra, degeneracy effect, exciton effect, space charge limited current, and unified mobility expression dependent on temperature, electric field and density, Three analytical iterative methods are proposed to solve the strong non-linear Poisson equation and the drift-diffusion equations. The method for the drift-diffusion equations involves introducing two constant coefficients and determining their values self-consistently by demanding the space averages of approximate drift and diffusion currents equal to the averages of accurate ones. The theoretical results for five high-efficiency OSCs are in good agreement with experimental data, including current-voltage curves, light intensity-dependent and open-circuit voltage () curves. The effects of energetic disorder in bulk heterojunction organic solar cells, and the sublinear relationship ∝ αin ( < 1) can be well explained. The Saha equation for exciton dissociation and the space-charge-limited-current (SCLC) effect are important for modelling high-efficiency OSCs. The ∼ relationship can be influenced by many factors. But, the ∼ relationship can be mainly and slightly influenced by the exciton effect and energetic disorder, respectively. When aiming to realize higher performance OSCs, one should decrease six material parameters, including the energetic disorder, exciton mass, deep level impurity concentration, the ratios of electron and hole mobilities, densities of states for electrons and holes, and potential barriers at the anode and cathode. The performance parameters of 15 triad compounds are predicted by using and absorption spectra from the literature along with other input parameters taken from previous optimized values, and the efficiency of two compounds was found to exceed 35%.
PubMed: 37800275
DOI: 10.1039/d3cp03366j -
Biomedical Chromatography : BMC Dec 2021Midostaurin (MDS) is used for the treatment of acute myeloid leukemia, myelodysplastic syndrome, and advanced systemic mastocytosis. MDS softgel capsule samples were...
Impurity profiling and stability-indicating method development and validation for the estimation of assay and degradation impurities of midostaurin in softgel capsules using HPLC and LC-MS.
Midostaurin (MDS) is used for the treatment of acute myeloid leukemia, myelodysplastic syndrome, and advanced systemic mastocytosis. MDS softgel capsule samples were subjected to stress testing per International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use guidelines for impurity profiling study. MDS underwent extensive degradation under stress testing (acid, alkaline, oxidative, photolytic, thermolytic, and hydrolysis conditions) and formed four degradation products (DPs). MDS and its DPs were separated well from one another with good resolution using reserved-phase HPLC using an Inertsil ODS-3V column (250 × 4.6 mm, 5 μm) and a mobile phase of ammonium formate (40 mM) and acetonitrile. The stability-indicating characteristic of the newly developed method was proven for the estimation of MDS assay, and its organic impurities were free from interference. The validated method exhibited excellent linearity, accuracy, precision, specificity, detection limit, and quantitation limit within 25 min run time. Stress testing, robustness, and solution stability were performed to ensure the continuous performance of the developed method. The peak fractions of DPs formed under stress testing were isolated and characterized using LC-MS, H and C NMR, IR, and UV-Vis. The structure of the major DPs was predicted as DP1 based on the spectral data. The proposed method is effectively used for MDS in bulk drug and finished formulations in the pharmaceutical industry.
Topics: Capsules; Chromatography, High Pressure Liquid; Drug Contamination; Limit of Detection; Linear Models; Mass Spectrometry; Reproducibility of Results; Staurosporine
PubMed: 34331472
DOI: 10.1002/bmc.5222