排序方式: 共有141条查询结果,搜索用时 15 毫秒
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Eslami Farnaz Pourayoubi Mehrdad Sabbaghi Fahimeh Dušek Michal Baniyaghoob Sahar Skořepová Eliška 《Crystallography Reports》2022,67(2):218-223
Crystallography Reports - For structures with a C2PO2 skeleton, a comparison of “single-and-half” phosphorus–oxygen bonds with single and double phosphorus–oxygen bonds is... 相似文献
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Hormoz Eslami Soleyman Hosseinzadeh Younes Saadat Faramarz Afshar-Taromi Mehdi Rimaz 《Colloid and polymer science》2012,290(14):1463-1469
In this work, the preparation of micron-sized polymer particles with nonspherical shapes via seeded dispersion polymerization of 2-ethylhexyl methacrylate (EHMA) with polystyrene (PS) seed particles in the presence of decane droplets and evaporation of decane after the polymerization under various polymerization conditions was discussed. The effect of monomer and decane content and polarity of the medium on the shape of the obtained particles was investigated. The experimental results showed that decreasing the amount of monomer and hydrocarbon volume of PEHMA/hydrocarbon domains, the particles decreased but they grew symmetrically, resulting in symmetric shapes. Furthermore, it was suggested that because of changing the solubility of the oligoradicals and hydrocarbon in the medium, the shape of the particles changed with changing the polarity of the medium. With decreasing the polarity of the medium, solubility of the oligoradicals in the medium increases and bigger polymer domains form on the surface of PS particles which can absorb higher amounts of decane. All of these can contribute to an increase in volume reduction after extraction of PEHMA/decane, resulting in various particle shapes. Further decreasing in polarity of the medium leads to an increase in the solubility of decane in the medium and decreasing the absorbed amount of decane by PS particles and PEHMA domains, resulting in lower volume reduction after evaporation of decane. 相似文献
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Nafise Modanlou Juibari Abbas Eslami 《Journal of Thermal Analysis and Calorimetry》2017,128(3):1327-1334
This work aimed the evaluation of pH influence in the obtainment of composites from palygorskite (PAL) and chitosan (CS). The materials PAL/CS-1 and PAL/CS-2 were obtained by similar methodology with modified pHs: 5.0 ± 0.5 and 11.0 ± 0.5, respectively. Both materials were evaluated for specific surface area analysis, elemental analysis, XRD, FTIR, thermal analysis, MEV and interaction drug composite, using 5-aminosalicylic acid (5-ASA) as model. The surface area analysis data showed the reduction in PAL/CS-2 related to CS presence on surface in contrast with PAL/CS-1, which corroborate with elemental analysis present nine times more of CS in PAL/CS-2 composition. Regarding to XRD data, the interaction of CS with PAL did not cause modification in clay structure in PAL/CS-2. These results were confirmed by FTIR data with the N–H deformation vibration in PAL/CS-2 while PAL/CS-1 was invariable to PAL. In thermal analysis, results were observed 60.2% residual mass to PAL/CS-2, which it was lower than PAL (87.2%) and PAL/CS-1 (86.7%), due to CS decomposition which had enthalpy energy of 62.1 J g?1 K?1, confirming the data previously cited. PAL/CS-2 presented 5-ASA adsorption of 7.9 mg g?1, which was inferior to others probably caused by scarcity of active sites of PAL already occupied by CS. These results showed that pH control was fundamental to enhance efficiency of obtainment of composite in basic pH because the decrease in CS protonation degree increasing interaction between this one and PAL, although it contributed to decrease in 5-ASA adsorption due to low availability of interaction sites. 相似文献
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Aluminum pillared and exchanged bentonite particles were synthesized by the ion exchange method. The characteristics of the particles were investigated by Fourier-transform infrared spectra (FTIR), X-ray diffraction (XRD), thermal gravimetric analysis (TGA), scanning electron microscope (SEM), electron dispersive X-ray spectrometer (EDS), reflectance spectrophotometer (RS) and electromagnetic transition instrument (ETI). FTIR spectra showed a successful incorporation of Al complexes into the clay interlayer. The TGA result demonstrated an improvement in thermal stability of the Al-pillared clay compared with the untreated particles. SEM and EDX results showed the presence of aluminum aggregates on the surface of clay. It was also found that Al ions affect electromagnetic properties of the clay particles. 相似文献
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Fe-pillared bentonite clay-based nanoadsorbent was synthesized by the thermal aging technique. The characteristics of the nanocomposite were detected by X-ray diffraction (XRD), Fourier transform infrared spectra (FTIR), thermal gravimetric analysis (TGA), scanning electron microscope (SEM), electron dispersive X-ray spectrometer (EDX), reflectance spectrophotometer (RS), and electromagnetic transition instrument (ETI). The TGA result demonstrated that the Fe particles generated on the clay surface can significantly improve the thermal stability of clay particles. The SEM and EDX results showed the presence of chemical elements of Fe, Al, and Si on the surface of clay. In this research, the successful synthesis of Fe-pillared clay nanocomposite can be concluded from the FTIR spectra. 相似文献
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We studied sensor application of a graphene oxide and hematite (α‐Fe2O3/GO) composite electrode well‐characterized by the SEM and XRD. Through differential pulse voltammetry (DPV), oxidation of dexamethasone sodium phosphate (DSP) was studied at the surface of a glassy carbon electrode (GCE) modified with graphene oxide nanosheets (GO) and the α‐Fe2O3/GO composite. The values of the transfer coefficient (α) and the diffusion coefficient (D) of DSP were 0.5961 and 4.71×10?5 cm2 s?1 respectively. In the linear range of 0.1–50 μM, the detection limit (DL) was 0.076 μM. In the second step, a GCE was modified with α‐Fe2O3/GO composite and the DSP measurement step was repeated to analyzed and compare the effects of hematite nanoparticles present on graphene oxide surfaces. According to the results, α and D were 0.52 and 2.406×10?4 cm2 s?1 respectively and the DL was 0.046 μM in the linear range of 0.1–10.0 μM. The sensor is simple, inexpensive and uses blood serum. 相似文献