Several important synthesis pathways for metal-organic frameworks (MOFs) were applied to determine how the synthesis methods and conditions affect the structure and adsorption capacity of the resulting samples. In the present work, three different synthesis routes were used to obtain copper trimesinate coordination polymer: Slow evaporation (A), solvothermal synthesis using a polyethylene glycol (PEG-1500) modulator (B), and green synthesis in water (C). This MOF was characterized by elemental analysis, infrared spectrometry, X-ray diffraction, scanning electron microscopy, thermogravimetry and volumetric nitrogen adsorption/desorption. The samples have permanent porosity and a microporous structure with a large surface area corresponding to the adsorption type I. The obtained MOF was tested as a sorbent to remove organic dyes methylene blue (МВ), Congo red (CR) and methyl violet (MV) as examples. Dye adsorption followed pseudo-first-order kinetics. The equilibrium data were fitted to the Langmuir and Freundlich isotherm models, and the isotherm constants were determined. Thermodynamic parameters, such as changes in the free energy of adsorption (∆G0), enthalpy (∆H0), and entropy (∆S0), were calculated. Thermolysis of copper trimesinate leads to the formation of carbon materials Cu@C with a high purity.
In recent decades, metal-containing nanocomposites have attracted considerable attention from researchers. In the present study, a detailed analysis of the preparation of Ag/C nanocomposites through the thermolysis of silver maleate was carried out. Thermolysis products are nanocomposites containing silver nanoparticles (NPs) uniformly distributed in a stabilizing carbon matrix. The composition, structure, and properties of the obtained nanocomposites were studied using IR-spectroscopy, X-ray diffraction (XRD), atomic force microscopy (AFM), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDS). This article reports on the possibility of using Ag/C nanocomposites to create new indicator papers that are sensitive to iodide ions in the concentration range of 0.03–1.6 mg/L (0.24–12.6 μM). The developed papers are used in a technique based on the oxidation of iodides with the formation of molecular iodine, which is extracted in an air stream and transferred to a sensitive paper layer containing silver NPs. The interaction of silver NPs with iodine leads to optical changes that can be tracked using a conventional scanner.
New complex based on cobalt (II) acrylate and 4′-phenyl-2,2′:6′,2″-terpyridine (PhTpy) was synthesized and characterized using a number of analytical techniques including IR and UV- vis spectroscopy, elemental, X-Ray and TGA/DSC analysis. The complex has high thermal stability and crystallinity. It is found that decomposition of the complex is accompanied by thermal polymerization of acrylic fragments that is a potential way for the preparation nanoparticles of metals or their oxides stabilized by the polymer matrix.
We report here our successful attempt to obtain self-healing supramolecular hydrogels with new metal-containing monomers (MCMs) with pendent 4-phenyl-2,2′:6′,2″-terpyridine metal complexes as reversible moieties by free radical copolymerization of MCMs with vinyl monomers, such as acrylic acid and acrylamide. The resulting metal-polymer hydrogels demonstrate a developed system of hydrogen, coordination and electron-complementary π–π stacking interactions, which play a critical role in achieving self-healing. Kinetic data show that the addition of a third metal-containing comonomer to the system decreases the initial polymerization rate, which is due to the specific effect of the metal group located in close proximity of the active center on the growth of radicals.
Metal-containing monomers based on maleates of copper and zinc, cinnamate of copper and acrylate of zinc with 4-phenyl-2,2′:6′,2′′-terpyridine ligand were prepared for the first time and characterized using a number of analytical techniques including infrared spectroscopy, elemental analysis and thermal gravimetric analysis. According to the results of the thermal analysis, the coordination mixed-ligand complexes based on zinc salts are more stable than copper one both in the case of monocarboxylic acids and dicarboxylic acids. The first stage of polymerization according to results of mass spectra of gaseous products is initiated in accordance with the Borodin–Hunsdiecker mechanism: the initial decarboxylation leads to the formation of carboxy biradicals, which, in turn, cause the polymerization and the formation of polymers. In this paper we also describe facile two-step Kröhnke-type synthesis of 4′-phenyl-2,2′:6′,2′′-terpyridine from 2-acetylpyridine and its NMR spectrum.
This study comprehensively investigates the efficiency of the formulation of tetraethoxysilane (TEOS) and 3-aminopropyltriethoxysilane (APTES) copolymer in sol-gel syntheses as part of a multivariate experiment. A methodology-based response surface was...
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