Thermo-physical Investigations of oils, N-(2-aminoethyl)oleamide and Resulting Gels using TGA-DSC

Edible vegetable oils were gelled by using N-(2-aminoethyl)-oleamide. Oils in their free state were subjected to differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) analysis. The gels of these oils were prepared by using N-(2-aminoethyl)-oleamide as gelator and similar thermal analysis of the gels was carried out. The thermal analysis data obtained was used to determine specific heat capacity at constant pressure (Cp). The values were compared with the reported values of heat capacities. It is observed that the thermal properties and transitions of oils and gels, specific heat capacity is helpful parameter to understand the fundamentals of gels and gelation strategies.

Preparation of Biodegradable and Low-Cost Lignin-Based PVOH Carbon Fibers Prepared by Electrospinning

A polyvinyl alcohol (PVOH)/lignin nanofiber was prepared by the electrospinning method as a precursor for biodegradable and low-cost carbon fibers. PVOH 15% was dissolved in water, and various concentration of lignin (5, 10, 15, 20, and 25%) was added. The presence of lignin in PVOH solution increased the viscosity and conductivity. From SEM analysis, PVOH solution produced smooth fiber, whereas the addition of lignin produced fibers in bead forms. The presence of lignin above 20% in PVOH did not produce spun-fiber. FTIR analysis confirmed that lignin was able to form hydrogen bonds with PVOH. TGA analysis showed that PVOH/lignin nanofibers had the highest residual mass, i.e., 40% at 600 °C. The morphology of the carbon fibers showed flake forms with many pores and had 58.07% carbon content.

How Ph.D. Students Start a Research

In education pedagogy, its necessary to prioritize tasks and jobs. Learn operating the reactor or required apparatus but most important first. Regarding measuring techniques (PSD measurement, pH measurement, XRD, SEM/EDS), learn more basic and fundamental techniques first followed by complimentary techniques. Regarding mineral carbonation, operation of reactor is a basic need followed by particle size measurement using Malvern Mastersizer and powders samples XRD analysis and identifying the phases and verifying those phases through TGA analysis. This article illustrates author personal research of 4 initial 4 months duration. Month wise progress is presented in this article in an interesting way.

Development and Characteristics of Multipurpose Transparent Polyurethane Film

In industry, recent research developments include flexible films and foldable films. The next step is the development of stretchable films, and studies are being intensively carried out. Research on the development of stretchable and transparent materials is also increasing greatly. Currently, polydimethylsiloxane (PDMS) is the most commonly used film in the industry. However, PDMS surfaces are hydrophobic, so their use is limited to making materials and compounds with hydrophilic properties. In this study, we developed a transparent polyurethane film that can be used for multiple purposes. A transparency comparison between the transparent polyurethane film and the general polyurethane film was used to verify their future application. The conventional polyurethane films showed a transmittance rate of 2.2 percent, but the transparent polyurethane films achieved a high transmittance rate of 85 percent. To determine whether the film can be realized, we produced a conductive paste using resin for the transparent polyurethane film. In addition, a conductive paste was made based on the material used in the transparent polyurethane film to verify the hardness and reliability of the adhesion of electrodes, and we confirmed this with thermogravimetric analysis (TGA). The transparent polyurethane based paste was made with stretchable electrodes through a screen printing method. The manufactured stretchable electrodes were demonstrated by mechanical and adhesion tests. Finally, a permittivity test was conducted to determine the suitability of the film for application to printed electrodes for antennas in the future. The genetic rate of transparent polyurethane films was better than that of conventional polyurethane films. Moreover, the adhesion of the transparent polyurethane film and stretchable electrodes was as good as that of conventional polyurethane film and stretchable electrodes, and observation by optical microscopy confirmed that the printing performance was also excellent. In addition, the conductive paste made based on the transparent polyurethane film material was cured for 1 hour at 120 °C, and TGA analysis confirmed that both the binders and curing agent responded well in the test for curing the developed stretchable electrodes and transparent polyurethane.

Treatment of Oil from the Oil Industry Wastewater by the Production of a Hydrophobic Magnetic Polymer Nanocomposites

A novel, economic and environment-friendly composite material based on magnetic hollow magnetite (Fe3O4) nanoparticle coated with a polyvinyl pyrrolidone (PVP) was produced to treat the oil from the oil industry wastewaters. The oils were readily removed via hydrophobic PVP -magnetite nanocomposite. In this study the physicochemical properties of the produced PVP-magnetite nanocomposite were investigated with Fourier transform infrared spectrophotometer (FTIR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA) analysis. The effects of increasing PVP -magnetite nanocomposite concentrations, the effects of separation time, effect of pH on the removal of oil were investigated. The removals of individual oil types with different carbon (C) ring numbers (from C 9 up to C 25) were investigated during oil removal. The reusing capacity of PVP-magnetite nanocomposite was investigated after 40 cycling for oil removal. The removal yields for all pollutants in the oil industry was investigated. FTIR analysis results showed that in the spectrum of PVP-coated magnetite nanocomposite the peak at 2500 1/cm can be attributed to the stretching vibration of C−N and C═O. XRD spectrum of the synthesized PVP– magnetite composite nanoparticle exhibited that the dominant phase of the composite nanoparticle is magnetite with a particle size of 16.8 nm. TGA analysis showed that about 69% weight loss was observed at 500°C and this is attributed to decomposition of PVP. Nonane (9 C rings) and undecane (11 C rings) have high removal yields like 99.99% while the oils with high carbon rings such as, 80% ducosene (22 C rings) and 72% pentacosane (25 C rings) exhibited low yields. The aforementined nanoparticle can be used 29 times to remove the oil with a yield of 99.99%. The maximum CODdis, COD, TSS and oil removal efficiencies were 99%, 99.5%, 99% and 99.90% respectively, via adsorption with 3 mg/l hydrophobic PVP-Fe3O4 / Polimer nanocomposite.

Biomass Fast Pyrolysis Vapor Upgrading over γ-Alumina, Hydrotalcite, Dolomite and Effect of Na2CO3 Loading: A Pyro Probe GCMS Study

The influence of γ-alumina, hydrotalcite, dolomite and Na2CO3 loaded γ-alumina, hydrotalcite, dolomite on fast pyrolysis vapor upgrading of beechwood was investigated using an analytical pyro probe-gas chromatography/mass spectrometry instrument (Py-GC/MS) at a temperature of 500 °C. Overall, this research showcased that these catalysts can deoxygenate biomass pyrolysis vapors into a mixture of intermediate compounds which have substantially lower oxygen content. The intermediate compounds are deemed to be suitable for downstream hydrodeoxygenation processes and it also means that hydrogen consumption will be reduced as a result of moderate in-situ deoxygenation. Among the support catalysts, the application of hydrotalcite yielded the best results with the formation of moderately deoxygenated compounds such as light phenols, mono-oxy ketones, light furans and hydrocarbons with a TIC area % of 7.5, 44.8, 9.8 and 9.8, respectively. In addition, acids were considerably reduced. Dolomite was the next most effective catalyst as γ-alumina retained most of the acids and other oxygenates. Na2CO3 loading on γ-alumina had a noticeable effect on eliminating more or less all the acids, enhancing the mono-oxy-ketones and producing lighter furans. In contrast, Na2CO3 loading on dolomite and hydrotalcite did not show a major impact on the composition except for further enhancing the mono-oxy-ketones (e.g., acetone and cyclopentenones). Additionally, in the case of hydrotalcite and γ-alumina, Na2CO3 loading suppressed the formation of hydrocarbons. In this research, the composition of pyrolytic vapors as a result of catalysis is elaborated further under the specific oxygenate groups such as acids, phenolics, furanics, ketones and acids. Further the catalysts were also characterized by BET, XRD and TGA analysis.

Structural Characterization of Thermally Stabilized Poly(acrylonitrile) Fibers by Means of X-ray Diffraction, FT-IR Spectroscopy, and TGA Analysis

The structure and effects of thermally stabilized PAN original fibers were characterized utilizing a mixture of volume density, color change observations, flame tests, X-ray diffraction (XRD), infrared spectroscopy (FT-IR), and thermogravimetric analysis (TGA) measurements. The results obtained from the analysis of XRD work showed the conversion of the original molecular structure from a highly laterally ordered condition to a disordered amorphous structure. The experimental results acquired from FT-IR analysis indicated rapid and concurrent aromatization and dehydrogenation reactions assisted by the formation of oxygen-containing functional groups. TGA analysis showed a carbon yield of 72% at 1000 °C. The application and use of NH4Br pretreatment are expected to increase the productivity of carbon fiber processing at lowered cost by significantly reducing the processing time necessary for the successful completion of thermal stabilization reactions.

POLYDENTATE ADSORBENT BASED ON LINEN CELLULOSE MODIFIED BY HYPERBRANCHED POLYESTER POLYBENZOYLTHIOCARBAMATE

A highly efficient hybrid adsorbent based on an industrially available, biodegradable, non-toxic linencellulose modified with hyperbranched polyesterpolybenzoylthiocarbamate has been synthesized.The synthesis was carried out using as a linkertoluene diisocyanate.The second-generation hyperbranched polyesterpolybenzoylthiocarbamate according to 1H, 13C NMR and IR spectroscopy contains 8 terminal benzoylthiocarbamate and 8 hydroxyl groups.In the first stage, the reaction of toluene diisociant with linen cellulose was carried out. By potentiometric titration, the content of toluene diisociant was found to be 27%. Then, hyperbranched polyesterpolybenzoylthiocarbamate was added to the modified linen cellulose. The content of hyperbranched polymer in cellulose, determined by the weight method, is 5%. Unreacted isocyanate groups are neutralized with isobutyl alcohol. The structure of the hybrid material is proven by IR spectroscopy. The adsorption properties of the polydentate adsorbent were studied with respect to Cu(II) ions. It was found that the adsorption capacity of the adsorbent is 6.93 mg/g. Using DSC and TGA analysis, the temperature characteristics, thermal effects, and mass loss of the obtained polydentate compound and its complexes were determined.It was shown that in an acidic medium at pH 3-4, desorption of Cu (II) and Co (II) ions occurs with the regeneration of a hybrid adsorbent.

Polyurethane-urea-amide-based triblock copolymer contains functionalized polystyrene: Synthesis, characterization and solvent resistivity study

Synthesized polystyrene (PSt) with a molecular weight of 2100 g/mol, hexamethylene diisocyanate (HMDI), 6-hexylamino benzamide (6B), and N1-(6-aminohexyl)-N4-(6-benzoylaminohexyl)terephthalamide (6T6B) are used to make a copolymer of thermoplastic elastomers. The prepared polymers’ inherent viscosity results (0.4–1.1 dL/g) support the polymer’s high mass. The presence of a monodentate urea group in the polymer chain is confirmed by FT-IR tests. The temperature dependence of FT-IR confirms that the synthesized copolymer has a space length dependent reversible crystallinity. Data from differential scanning calorimetry (DSC) also shows that the hard segment crystallization is strong and reversible in nature. The XRD results show that the polymer is semi-crystalline. The TGA analysis confirmed that the synthesized copolymers are thermally stable up to 290°C. The presence of hydrogen bonds in polymer chains is thermally reversible. The polymer’s solvent resistivity is excellent due to its high crystallinity.