ABSTRACT
The design and manufacture of innovative multifunctional materials possessing superior characteristics, quality and standards, rigorously required for future development of existing or emerging advanced technologies, is of great importance. These materials should have a very low degree of influence (or none) on the environmental and human health. Adjusting the properties of epoxy resins with organophosphorus compounds and silver-containing additives is key to the simultaneous improvement of the flame-resistant and antimicrobial properties of advanced epoxy-based materials. These environmentally friendly epoxy resin nanocomposites were manufactured using two additives, a reactive phosphorus-containing bisphenol derived from vanillin, namely, (4-(((4-hidroxyphenyl)amino)(6-oxido-6H-dibenzo[c,e][1,2]oxaphosphinin-6-yl)methyl)-2-methoxyphenyl) phenylphosphonate (BPH), designed as both cross-linking agent and a flame-retardant additive for epoxy resin; and additional silver-loaded zeolite L nanoparticles (Ze-Ag NPs) used as a doping additive to impart antimicrobial activity. The effect of BPH and Ze-Ag NPs content on the structural, morphological, thermal, flame resistance and antimicrobial characteristics of thermosetting epoxy nanocomposites was investigated. The structure and morphology of epoxy nanocomposites were investigated via FTIR spectroscopy and scanning electron microscopy (SEM). In general, the nanocomposites had a glassy and homogeneous morphology. The samples showed a single glass transition temperature in the range of 166-194 °C and an initiation decomposition temperature in the range of 332-399 °C. The introduction of Ze-Ag NPs in a concentration of 7-15 wt% provided antimicrobial activity to epoxy thermosets.
ABSTRACT
In order to obtain highly active catalytic materials for oxidation of carbon monoxide and volatile organic compounds (VOCs), monometallic platinum, copper, and palladium catalysts were prepared by using of two types of ZSM-5 zeolite as supports-parent ZSM-5 and the same one treated by HF and NH4F buffer solution. The catalyst samples, obtained by loading of platinum, palladium, and copper on ZSM-5 zeolite treated using HF and NH4F buffer solution, were more active in the reaction of CO and benzene oxidation compared with catalyst samples containing untreated zeolite. The presence of secondary mesoporosity played a positive role in increasing the catalytic activity due to improved reactant diffusion. The only exception was the copper catalysts in the reaction of CO oxidation, in which case the catalyst, based on untreated ZSM-5 zeolite, was more active. In this specific case, the key role is played by the oxidative state of copper species loaded on the ZSM-5 zeolites.
ABSTRACT
The present study is aimed at investigations on the catalytic activity for total oxidation of volatile organic compounds (VOCs), such as toluene, acetone, n-hexane and dichlorobenzene onto zeolite-like materials synthesized from coal fly ash (FA) directed to development of an economically efficient approach for degradation of VOCs. Fly ash zeolites (FAZ) were prepared by alkaline conversion of FA collected from Thermal Power Plants supplied with lignite coal from "Maritza-East" basin in Bulgaria. Different synthesis procedures double stage fusion-hydrothermal activation, fusion-atmospheric crystallization and atmospheric aging were applied. The synthesis products were identified by X-ray diffraction, and were assigned to zeolite Na-X. Scanning electron microscopy images reveal submicron dimensions of the composing crystallites. Nitrogen adsorption/desorption measurements reveal a mixed micro-mesoporous structure and specific surface area between 116 and 396â¯m2/g for the obtained FAZ. Relationships between surface properties, iron content and the catalytic activity of FAZ were investigated and discussed. Copper-modified fly ash zeolites (Cu-FAZ) were prepared by incipient wetness impregnation technique with copper acetylacetonate. The loading of 5â¯wt. % copper on the zeolite samples was achieved. The catalytic activity of FAZ and Cu-FAZ in the total oxidation of model VOCs mixture containing n-hexane, acetone, toluene, 1,2 dichlorobenzene was evaluated.
ABSTRACT
Human bestrophin-1 (hBest1) is a transmembrane calcium-activated chloride channel protein - member of the bestrophin family of anion channels, predominantly expressed in the membrane of retinal pigment epithelium (RPE) cells. Mutations in the protein cause ocular diseases, named Bestrophinopathies. Here, we present the first Fourier transform infrared (FTIR) study of the secondary structure elements of hBest1, π/A isotherms and hysteresis, Brewster angle microscopy (BAM) and atomic force microscopy (AFM) visualization of the aggregation state of protein molecules dispersed as Langmuir and Langmuir-Blodgett films. The secondary structure of hBest1 consists predominantly of 310-helices (27.2%), α-helixes (16.3%), ß-turns and loops (32.2%). AFM images of hBest1 suggest approximate lateral dimensions of 100×160Å and 75Å height. Binding of calcium ions (Ca2+) induces conformational changes in the protein secondary structure leading to assembly of protein molecules and changes in molecular and macro-organization of hBest1 in monolayers. These data provide basic information needed in pursuit of molecular mechanisms underlying retinal and other pathologies linked to this protein.
