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Fe3O4-SiO2-NH2, Fe3O4-CTABSiO2-NH2 and Fe3O4-SiO2-CTABSiO2-NH2 magnetic adsorbents were successfully prepared and could be used effectively for the adsorption of Light Green from aqueous solutions. Unlike the first sample, mesoporous silica coatings were created using cetyltrimethylammoniumbromide micelles as molecular templates on superparamagnetic iron oxide in one sample, and on silica-coated iron oxide in the other sample to improve the adsorptive properties of the nanocomposites. The characterization by FT-IR, SEM/EDX, Zeta-potential, XRD, VSM, and N2-adsorption/desorption confirmed the production of mesoporous silica layer. Although coating processes with both silica and mesoporous silica layers led to a vaguely decrease in saturation magnetization of the Fe3O4-SiO2-CTABSiO2-NH2, the nanoparticles were protected with silica coatings for environment conditions and made more suitable for subsequent amino functionalization. The results determined from Batch adsorption experiments fitted to Langmuir isotherm model with maximum adsorption capacity (qmax) equal to 56.18, 196.08 and 227.27 mg g−1, for Fe3O4-SiO2-NH2, Fe3O4-CTABSiO2-NH2 and Fe3O4-SiO2-CTABSiO2-NH2, respectively, and it was seen from the kinetic results, the LG adsorption was identified by pseudo-second-order kinetics, revealing that LG adsorption process is homogeneous, monolayer and based on chemical interactions. According to the results, both silica and mesoporous silica coating strategy can play crucial role in improving the adsorptive properties of nanocomposites.

Multifunctional magnetic mesoporous nanocomposites are promising materials to remove the various pollutants from water due to the remarkable properties such as multiple binding sites, high surface area, and magnetic separation. Herein, we have developed a versatile nanocomposite, in which polydopamine (PDA) coated Fe3O4 nanoparticles are introduced during the synthesis of SBA-15 matrix for the first time to enhance adsorptive properties of hydrophilic magnetic mesoporous nanocomposite by combining the properties of high surface area, magnetization, and capability of interacting with more functional groups in one material. The resulting nanocomposite, Fe3O4@PDA@SBA-15, has been proved to be the effective sorbent for the removal of cationic dye, which can be ascribed to the functional groups of grafted PDA and the textural features of matrix SBA-15. On the other hand, after chemical modification via silanization of vinyltriethoxysilane (VTES), Fe3O4@PDA@SBA-15 nanocomposite turned to be a hydrophobic material, Fe3O4@PDA@SBA-15@VTES, which can adsorb oil with high adsorption capacity which could reach 8.83 times of its own weight. Moreover, both nanocomposites could be recycled by facile washing and drying processes. The materials provide a simple strategy for the preparation of multifunctional magnetic mesoporous nanocomposites satisfying various applications in water treatment.

Fe3O4@SiO2@NH2 nanocomposite was prepared for highly effective adsorption of two anionic dyes one of which is triarylmethane dye (light green, LG) and the other is azo dye (brilliant yellow, BY). T...

WOS: 000449033200003, In our approach for magnetic iron oxide nanoparticles surface modification, the fabrication of an inorganic shell, consisting of silica by the deposition of preformed colloids onto the nanoparticle surface and functionalization of these particles, was realized. The magnetic nanoparticles, non-coated and coated with silica layer by Stober method, are functionalized with chlorosulfonic acid. The magnetic nanoparticles (MNPs), in size of 10-13 nm, could be used as acid catalyst in biodiesel production and show superparamagnetic character. The prepared nanoparticles were characterized by different methods including XRD, EDX, FT-IR and VSM. The catalytic activity of the coated and non-coated solid acids was examined in palmitic acid-methanol esterification as an industrial reaction for biodiesel synthesis. Although thin silica layer results in only a minor obstacle with respect to magnetism, it can accelerate the mass transportation due to its relatively porous structure and magnetic core may be more stable in the acidic reaction medium by means of covering process. Accordingly, coating strategy can be efficient way for allowing applications of MNPs in acid catalyzed esterification., Commission of Scientific Research Projects of Uludag University [KUAP(F)-2014/33], This work was supported by The Commission of Scientific Research Projects of Uludag University, Project number: KUAP(F)-2014/33.

WOS: 000324103300007, The influence of poly(ethylene glycol) (PEG) and synthesis temperature in the synthesis of SBA-15-SO3H was investigated to evaluate the catalytic activity in the esterification of propionic acid with methanol. The catalysts were characterized by means of surface and structure analyses; X-ray diffraction, FT-IR, scanning electron microscopy, Thermo-gravimetric and N-2 adsorption/desorption techniques. It was found that, by the addition of PEG, the surface area and porosity of SBA-15-SO3H increased, while the structure and size of mesopores remained unchanged. Nitrogen sorption measurements indicate that PEG introduces additional pores into the pore walls of SBA-15-SO3H. Thus, a simple way of improving the porosity of mesoporous SBA-15-SO3H was presented that could enhance transport of substrates through the porous system and allow the generation of stable mesoporous replicas, important for catalytic applications and also beneficial for replication and nanocasting purposes., Commission of Scientific Research Projects of Uludag University [UAP(F)-2011/69], This work was supported by The Commission of Scientific Research Projects of Uludag University, Project number: UAP(F)-2011/69.

Magnetic vinylphenyl boronic acid microparticles, poly(ethylene glycol dimethacrylate-vinylphenyl boronic acid) [m-poly(EGDMA-VPBA)], produced by suspension polymerization, was found to be efficient solid acid catalyst for the esterification of methanol and propionic acid. Characterization techniques such as FT-IR, Elemental analyses, ICP-AES, ESR, SEM and N 2 sorption showed that both of Fe 3 O 4 and H 2 SO 4 are bonded to the polymer successfully. Esterification was studied for different molar percentages of H 2 SO 4 at temperature range of 50-70 o C. The apparent activation energy was found to be 27.7 kj.mol -1 for 10% H 2 SO 4 doped m-poly(EGDMA-VPBA). Combining of strong acid H 2 SO 4 with m-poly(EGDMA-VPBA), leads to materials with different functional properties. In addition, H 2 SO 4 species could be introduced into the structure as acid centers, therefore this micro-dimensional catalyst has potential candidate for applications in the catalytic esterifications such as propionic acid with methanol.

The magnetic-poly(divinylbenzene-4-vinylpyridine) [m-poly(DVB-4VP)] microbeads (average diameter: 180–212 μm) were synthesized by copolymerizing of divinylbenzene (DVB) with 4-vinylpyridine (4VP) and by mixing this copolymer with Fe 3 O 4 nanoparticles. The resultant material was characterized by N 2 adsorption/desorption, ESR, elemental analysis, scanning electron microscope (SEM) and swelling studies. After functionalized with sulfonic acid, m-poly(DVB-4VP-SO 3 H) was characterized by FT-IR and TGA analysis. The results showed that both of Fe 3 O 4 and –SO 3 H are bonded to the polymer successfully. N 2 adsorption/desorption isotherms of synthesized samples had the hysteresis behaviour associated with mesoporous materials (pore diameter: 3.73 nm). Sulfonic acid functionalized mesoporous m-poly(DVB-4VP-SO 3 H) has been demonstrated to have higher reactivity than commercially available solid acid catalysts for the conversion of propionic acid to methyl ester. The apparent activation energy was found to be 38.5 kJ mol −1 for m-poly(DVB-4VP-20%SO 3 H). The catalyst showed negligible loss of activity after four repetitive cycles.

Kinetics of heterogeneous catalysed esterification of propionic acid with n-amyl alcohol was studied with a microporous cation-exchange resin catalyst, Dowex 50Wx4, in a stirred batch reactor to synthesise amyl propionate. Effects of various parameters such as speed of agitation, catalyst loading, and reaction temperature on reaction rate were investigated. The equilibrium conversion of propionic acid increased with in catalyst loading and reaction temperature. Stirrer speed had virtually no effect on the reaction rate under the experimental conditions. The apparent activation energy was found to be 43.167 kJmol−1 for the formation of amyl propionate and the equilibrium constant, which is independent of temperature ranging from 318 to 348 K, was found to be 4.05. It was also observed that the initial reaction rate decreased with water concentrations and increased with that of acid and increased with that of alcohol linearly. The reaction was found to occur between an adsorbed acid molecule and a molecule of alcohol in the bulk and it was concluded that the reaction mechanism can be represented by Eley-Rideal model.

Esterifications of n-amyl alcohol with propionic acid catalyzed by macroporous (Amberlyst-15) and microporous (Dowex 50 W and Amberlite IR-120) polymeric ion-ex6hange resins were carried out between 333-348 K. When these catalysts were used as commercially available, Amberlyst-15 was observed to be the most effective catalyst with respect to rate constants, but after drying it became the less effective one. The reaction rate increased with increase in catalyst concentration and reaction temperature. Stirrer speed and different mesh sizes had virtually no effect on the rate under the experimental conditions. The effect of divinylbenzene content was examined for the micro porous resin Dowex 50 W, and the results showed that the propionic acid conversion decreased as the divinylbenzene content was increased. The rate data were correlated with a second-order homogeneous reaction model. The apparent activation energies, reaction enthalpies and entropy values were calculated for each catalyst. Reaction monitoring is simple and fast by volumetric method and the reproducibility of this method was the order of +/- %2.54.