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首页> 外文期刊>Arabian Journal for Science and Engineering >Characterization of Caesium Carbonate‑Doped Porous Non‑Activated Graphitic (Hexagonal) Boron Nitride and Adsorption Properties
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Characterization of Caesium Carbonate‑Doped Porous Non‑Activated Graphitic (Hexagonal) Boron Nitride and Adsorption Properties

机译:碳酸铯掺杂多孔非活性石墨(六边形)氮化物和吸附性能的表征

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In this study, the effect of caesium carbonate with a balanced strong base characteristic on the morphology crystallinity,porosity and specific surface area of graphitic boron nitride is reported. The mass ratio of caesium carbonate was adjusted as0.9 and 1.2 at the constant mass of urea and B_2O_3in a mixture of 2 g and 1 g, respectively. The products were characterizedby using infrared spectroscopy (FTIR), powder X-ray diffraction analysis (XRD), scanning electron microscopy (SEM),energy-dispersive X-ray spectroscopy (EDS), high-resolution transmission electron microscopy (HR-TEM) and specificsurface area (SSA) and porosity analysis. gBN formation determined by XRD analysis was accelerated and improved orderedlateral polymorph in which graphitization index was found to be very close to the graphite as 2.02 and 1.84 as for 0.9 and1.2 g dopant level, respectively. The average grain size of the synthesized undoped, 0.9 and 1.2 g caesium carbonate-dopedsamples had 3.61, 10.84 and 12.00 nm, respectively. The porous nature of the product has been confirmed by the SEM andevolution of gaseous material from the surface. The EDX results reveal that the elements used for the preparation of samplesdistribute homogeneously and neither caesium nor carbon atoms enter into the crystal structure indicating the purity ofsamples. The SSA and porosity parameters are found to be about 77.1 m~2/g and 0.1–100 nm range, respectively. Caesiumcarbonate propagated the graphitic nature and crystallinity of BN at a lower temperature than O’Connor method due to risein electronic interaction as a basic compound.
机译:在这项研究中,碳酸铯对形态结晶度的平衡良好碱性特征的影响,报道了石墨硼氮化物的孔隙率和比表面积。将碳酸铯的质量比调节为0.9和1.2在urea和b_2o_3的恒定质量下分别在2g和1g的混合物中。产品的特征在于通过使用红外光谱(FTIR),粉末X射线衍射分析(XRD),扫描电子显微镜(SEM),能量分散X射线光谱(EDS),高分辨率透射电子显微镜(HR-TEM)和特定表面积(SSA)和孔隙度分析。通过XRD分析确定的GBN形成加速和改进了有序的侧向多晶型物,其中发现石墨化指数非常靠近石墨,为0.9和1.84,为0.9和1.2克掺杂剂水平。合成的平均晶粒尺寸未掺杂,0.9和1.2g碳酸铯掺杂样品分别具有3.61,10.84和12.00nm。产品的多孔性质已被SEM和SEM确认从表面的气态材料的演变。 EDX结果表明,用于制备样品的元素均匀地分配铯,碳原子都不进入晶体结构,表明纯度样品。发现SSA和孔隙度参数约为77.1 m〜2 /g和0.1-100nm的范围。铯碳酸盐在较低的温度下繁殖Bn的石墨性质和结晶度,而不是由于升高而比O'connor方法在电子互动中作为基本化合物。

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