Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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Article Citation - WoS: 17Citation - Scopus: 23Synthesis of Zinc Borate by Inverse Emulsion Technique for Lubrication(Springer Verlag, 2011) Atakul Savrık, Sevdiye; Balköse, Devrim; Balköse, Devrim; Ülkü, Semra; 03.02. Department of Chemical Engineering; 03. Faculty of Engineering; 01. Izmir Institute of TechnologyLubricating oil additives based on boron compounds are promising materials for lubrication due to their tribological advantages such as antiwear efficiency, good film strength, and high temperature resistance. This article deals with the preparation of zinc borate particles that are well dispersed and colloidally stabilized in mineral oil. This method starts with preparing two inverse emulsions (water-in-oil) with sorbitan monostearate (Span 60) as a surfactant, light neutral oil as a continuous phase, and the aqueous solutions of borax decahydrate (Na2B4O7·10H 2O) and zinc nitrate (Zn(NO3)2·6H 2O) as the dispersed phases. The produced particles were zinc borate crystals having both rod-like and spherical morphologies, and the diameters of spherical particles were changing between 20 and 30 nm. FTIR spectra of the obtained particles showed the characteristic peaks of trihedral borate (B(3)-O) and tetrahedral borate (B(4)-O) groups as well as the specific peaks of the sorbitan monostearate. TG showed 30.42% and 22.08% mass loss at 600 °C for the samples prepared by inverse emulsion and precipitation techniques, respectively. The endothermic peak at 50 °C is observed due to the melting of sorbitan monostearate and the heat of melting is evaluated as -3.50 J/g. Tribological studies revealed that sorbitan monostearate not only outperformed as a dispersing agent of inorganic particles, but also it proved to be an anti-wear agent. Zinc borate produced by precipitation decreased the wear scar diameter from 1.402 to 0.639 mm and the friction coefficient from 0.099 to 0.064. The inverse emulsion was effective in decreasing wear scar diameter and the friction coefficient by lowering them to 0.596 and 0.089 mm, respectively.Article Citation - WoS: 11Citation - Scopus: 15Supercritical Carbon Dioxide Drying of Methanol-Zinc Borate Mixtures(American Chemical Society, 2009) Gönen, Mehmet; Balköse, Devrim; Balköse, Devrim; Ülkü, Semra; Ülkü, Semra; 03.02. Department of Chemical Engineering; 03. Faculty of Engineering; 01. Izmir Institute of TechnologySupercritical carbon dioxide (CO 2) drying of zinc borate species was investigated to evaluate possible chemical alterations in the product during the drying. Methanol-wetted zinc borates produced either from borax decahydrate and zinc nitrate hexahydrate (2ZnO · 3B 2O 3 ·7H 2O) or from zinc oxide and boric acid (2ZnO · 3B 2O 3 ·3H 2O) were dried by both conventional and supercritical carbon dioxide drying methods. Zinc borate samples dried by both techniques were characterized using analytical titration, X-ray powder diffraction (XRD), thermo gravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy, elemental analysis, and scanning electron microscopy (SEM). It was found that while zinc borate obtained from zinc oxide and boric acid did not have any chemical interaction with CO 2, carbonates were formed on the surface of zinc borate obtained from borax decahydrate and zinc nitrate hexahydrate. The main factor for the carbonate formation during supercritical CO 2 drying is anticipated as the structural differences of zinc borate species. CO 2 is a nonpolar solvent, and it does not usually react with polar substances unless water is present in the medium. While 2ZnO · 3B 2O 3 ·3H 2O had three bound OH groups, 2ZnO · 3B 2O 3 ·7H 2O had five bound OH groups and one mole of water of crystallization. It is proposed that the water of crystallization reacts with CO 2 forming carbonic acid. Then, carbonic acid, which is stronger than boric acid, substitutes borate ions from their zinc salts.