Imidacloprid (I) and thiamethoxam (T) are widely used neonicotinoid insecticides with high persistence in the environment and thus included in the watch list of substances for European Union-wide monitoring reported in the Decision 2015/495/EU. In this work aqueous solutions of I, T and I?+?T were subjected to advanced oxidation by air plasma produced by negative DC corona discharges above the liquid surface. The oxidative degradation of each pollutant was investigated by monitoring the rate and the products of its decay when treated alone and in the presence of variable amounts of the other compound. The results show that both I and T are readily degraded and that mineralization can be achieved in this process, as proven by the measurement of the residual organic carbon and by the quantitative conversion of chlorine and sulfur into inorganic chloride and sulfate, respectively. The major organic intermediates formed during the complex stepwise oxidation of I and T were identified and monitored by HPLC–MS/MS analysis. The results of kinetic studies show that both for I and T the reaction rate depends inversely on the insecticide initial concentration, that I and T have similar reactivities and that they do not interfere reciprocally in any specific way when treated in mixture at a total concentration of ca 1?×?10?4 M. Based on literature data and on previous results with the same reactor, it is reasonable to propose that the oxidation of I and T is initiated by the reaction with OH radicals.
Thermosensitive‐thermochromic pigments are classified as smart materials capable of detecting and/or responding to environmental stimuli, and specifically in this study, changes in temperature that induce a change in the color of the material. This study aims to obtain nanoparticles of poly(styrene‐co‐butyl acrylate) and poly(styrene‐co‐methyl methacrylate), containing thermosensitive‐thermochromic pigments that are incorporated into the monomer droplets in miniemulsion polymerization. Miniemulsion polymerization has the advantage that the pigment particles can be dispersed directly in the monomer droplets and are encapsulated when the miniemulsion droplets are polymerized. Using controlled/living radical polymerization (or Reversible Deactivation Radical Polymerization), it is possible to produce polymers with better control of microstructure and narrower molecular weight distributions. Nitroxide‐mediated polymerization (NMP) is conducted using the BlocBuilder initiator, as well as a conventional free radical polymerization (FRP) using potassium persulfate (KPS) and 2,2‐azobis(2‐methylpropionitrile) (AIBN). Stable latexes containing the thermosensitive‐thermochromic pigments are obtained by both NMP and FRP. Films are made from the latexes and shown to exhibit thermochromic behavior. 相似文献
A novel bidentate Schiff base ligand (L) and some d‐transition metal chelates (Cr (III), Mn (II), Fe (III), Co (II), Ni (II), Cu (II), Zn (II) and Cd (II)) were synthesized and characterized using various physicochemical and spectroscopic techniques like elemental analysis, IR, mass, UV–visible and thermal analysis. The spectroscopic data suggested that the parent Schiff base ligand coordinated to the metal ions through both imine nitrogen atoms. The molecular and electronic structure of the free ligand was optimized theoretically, and the quantum chemical parameters were calculated. The molecular structure can be used to investigate the coordination sites and the total charge density around each atom. The free ligand and its complexes were screened for their antimicrobial activities for various pathogenic bacteria and fungi. The anticancer activities of the free ligand, Cr (III), Mn (II) and Fe (III) complexes were screened against MCF‐7 cell line and found that Mn (II) complex has the lowest IC50 (15.90 μg/ml). Molecular docking was used to predict the binding between the free ligand with receptor of mutant human androgen (ARccr) derived from androgen‐independent prostate cancer (1GS4), crystal structure of yeast‐specific serine/threonine protein phosphatase (ppz1) of Candida Albicans (5JPE) and crystal structure of renal tumor suppressor protein, folliculin (3 V42) and to identify the binding mode and the crucial functional groups interacting with the three proteins. 相似文献
Summary: The growth of surface‐initiated poly([2‐(methacryloyloxy)ethyl]trimethylammonium chloride) (pMETAC) brushes by ATRP was monitored by the quartz crystal microbalance technique with dissipation (QCM‐D). The change in mass of the quartz crystals starting from the adsorption of a thiol initiator monolayer through to the growth of the polymer brushes was determined. The use of QCM‐D allowed determination of the kinetics of polymerization from the surface. The technique can be applied to other polymers synthesised from surfaces and allows the study of varying conditions on the polymerization kinetics.
Changes in frequency of a quartz crystal during polymerization. 相似文献
The increase of energy demand added to the concern for environmental pollution linked to energy generation based on the combustion of fossil fuels has motivated the study and development of new sustainable ways for energy harvesting. Among the different alternatives, the opportunity to generate energy by exploiting the osmotic pressure difference between water sources of different salinities has attracted considerable attention. It is well-known that this objective can be accomplished by employing ion-selective dense membranes. However, so far, the current state of this technology has shown limited performance which hinders its real application. In this context, advanced nanostructured membranes (nanoporous membranes) with high ion flux and selectivity enabling the enhancement of the output power are perceived as a promising strategy to overcome the existing barriers in this technology. While the utilization of nanoporous membranes for osmotic power generation is a relatively new field and therefore, its application for large-scale production is still uncertain, there have been major developments at the laboratory scale in recent years that demonstrate its huge potential. In this review, we introduce a comprehensive analysis of the main fundamental concepts behind osmotic energy generation and how the utilization of nanoporous membranes with tailored ion transport can be a key to the development of high-efficiency blue energy harvesting systems. Also, the document discusses experimental issues related to the different ways to fabricate this new generation of membranes and the different experimental set-ups for the energy-conversion measurements. We highlight the importance of optimizing the experimental variables through the detailed analysis of the influence on the energy capability of geometrical features related to the nanoporous membranes, surface charge density, concentration gradient, temperature, building block integration, and others. Finally, we summarize some representative studies in up-scaled membranes and discuss the main challenges and perspectives of this emerging field.Advanced nanostructured membranes with high ion flux and selectivity bring new opportunities for generating clean energy by exploiting the osmotic pressure difference between water sources of different salinities.相似文献
Kinetic resolution is achieved in the reaction of racemic diiron complexes like 1 with the chiral nitrone (−)- 2 . Oxidative removal of the metal and reductive cleavage of the N−O bond provides β-amino acids. This sequence was used in the synthesis of β-amino acids as well as the corresponding β-lactams 4 (via 3 ). 相似文献
The present study focuses on the possible involvement of l-arginine-nitric oxide-cGMP-ATP-sensitive K+ channel pathway in the antinociceptive activity of a novel diarylpentanoid analogue, 2-benzoyl-6-(3-bromo-4-hydroxybenzylidene)cyclohexen-1-ol (BBHC) via a chemical nociceptive model in mice. The antinociceptive action of BBHC (1 mg/kg, i.p.) was attenuated by the intraperitoneal pre-treatment of l-arginine (a nitric oxide synthase precursor) and glibenclamide (an ATP-sensitive K+ channel blocker) in acetic acid-induced abdominal constriction tests. Interestingly, BBHC’s antinociception was significantly enhanced by the i.p. pre-treatment of 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ), a selective inhibitor of soluble guanylyl cyclase (p < 0.05). Altogether, these findings suggest that the systemic administration of BBHC is able to establish a significant antinociceptive effect in a mice model of chemically induced pain. BBHC’s antinociception is shown to be mediated by the involvement of l-arginine-nitric oxide-cGMP-ATP-sensitive K+ channel pathway, without any potential sedative or muscle relaxant concerns. 相似文献