Galvanic sludge results from the treatment of effluents generated by the industrial metal surface treatment of industrial material, which consists in the deposition of a metal on a surface or a metal surface attack, for example, electrodeposition of conductors (metals) and non conductive, phosphate, anodizing, oxidation and/or printed circuit. The treatment proposed here is exposure of the galvanic sludge to the high temperatures provided by thermal plasma, a process which aims to vitrify the galvanic sludge and render metals (iron, zinc, and chromium) inert. Two different plasma reactors were assembled: with a DC transferred arc plasma torch and with a DC nontransferred arc plasma torch. In this way it was possible to verify which reactor was more efficient in the inertization of the metals and also to investigate whether the addition of quartzite sand to the sludge influences the vitrification of the material. Quantification of water content and density of the galvanic raw sludge were performed, as well as analyzes of total organic carbon (TOC) and identify the elements that make up the raw sludge through spectroscopy X-ray fluorescence (XRF). The chemical composition and the form of the pyrolyzed and vitrified sludge were analyzed by scanning electron microscopy with energy-dispersive X-ray spectrometer (SEM-EDS) analysis, which it is a analysis that shows the chemical of the sample surface. The inertization of the sludge was verified in leaching tests, where the leachate was analyzed by flame atomic absorption spectroscopy (FAAS). The results of water content and density were 64.35% and 2.994 g.cm(-3), respectively. The TOC analysis determined 1.73% of C in the sample of galvanic raw sludge, and XRF analysis determined the most stable elements in the sample, and showed the highest peaks (higher stability) were Fe, Zn, and Cr. The efficiency of the sludge inertization was 100% for chromium, 99% for zinc, and 100% for iron. The results also showed that the most efficient reactor was that with the DC transferred arc plasma torch and quartzite sand positively influenced by the vitrification during the pyrolysis of the galvanic sludge.
In this study, we describe the synthesis of amides and evaluate their use as slip additive agents in polypropylene films. The additives N-isopropyl-stearamide and N,N-diisopropyl-stearamide were synthesized and characterized and then used to prepare masterbatches. Erucamide, a commercial masterbatch, was used as the reference standard. A 32 factorial experimental design was used to create the different compositions of slip additives in polymer films. The films were processed via flat-die extrusion and stored in an oven at a constant temperature of 40 °C for seven days. The following are the properties evaluated in the study: thermal decomposition temperature, fusion temperature, fusion enthalpy, coefficient of friction, surface energy, contact angle, and seal initiation temperature. The results were evaluated by analysis of variance (ANOVA) at a 90 % confidence interval. The analysis of the results showed that N-isopropyl stearamide and N,N-diisopropyl stearamide do not provide an adequate surface slip for polypropylene films at the conditions used in the study. In turn, at the same conditions, erucamide, the commercial amide, also does not provide the required surface energy for printing and lamination processes required for polypropylene films.
The synthesis is described of new liquid crystalline heteroaromatic compounds containing the five-membered isoxazole, tetrazole and 1,2,4-oxadiazole rings. Two liquid crystalline series including five-membered heterocycles were synthesized. The compounds with the mesogenic units tetrazole and isoxazole (Series I) showed nematic and smectic C phases, while the compounds with the units tetrazole and 1,2,4-oxadiazole (Series II) presented nematic (N), smectic C (Sm C ), and smectic A (Sm A ) mesophases. The transition temperatures and textures of the mesophases determined were characterized using polarized optical microscopy.
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