Thermokinetic parameters of the primary coal tars destruction in the presence of catalysts and polymeric materials

N. Balpanova, M. Baikenov, A. M. Gyulmaliev, Z. Absat, Zh. Batkhan, F. Ma, K. Su, S.V. Kim, G. Baikenova, D. Aitbekova, A. Tusipkhan
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引用次数: 1

Abstract

The hydrogen-donor abilities of polymers and the activity of catalysts in the process of thermal destruction of the organic mass of primary coal tar (PCT) are studied by non-isothermal kinetics methods. PCT,magnetic microspheres, nickel-deposited chrysotilechrysotile and Fe3O4nanocatalysts were used as initial raw materials. Рolymers such as polyethylene (PE), polystyrene(PS) and polyethylene glycol (PEG) were selected as a hy-drogen donor. The phases Mg3[OH]4{Si2O5} and NiO were determined by X-ray phase analysis (XRD) in the obtained catalyst (nickel-deposited chrysotile), and the presence of highly dispersed nickel oxide particles on the surface and inside the nanotubes was shown by the transmission electron microscope (TEM). Nickel oxide particles of 8–11 nmand 30–37 nmwere evenly distributed on the surface and inside the chrysotile nanotubes. The kinetic parameters of the thermal destruction of a mixture of PCT, catalyst and polymer material were determined on the basis of thermogravimetric analysis using the integral method and the method for determin-ing the thermokinetic parameters by the inflection point on the thermogravimetric curve(TG). The change in the activation energy, rate constant and pre-exponential factor with an increase in the degree of destruction of the organic mass of the PCT is established. It was shown that the nature of polymers and catalysts significantly affects the value of the rate constant and the activation energy. The calculated activation energies of the thermal destruction of a mixture of coal tar with PS and PE in the presence of a catalyst (nickel-deposited chrysotile) by the first method are 47.6 kJ/mol and 40.4 kJ/mol, and by the second method are 47.3 kJ/mol and 86.5kJ/mol respectively.
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催化剂和高分子材料存在下初生煤焦油破坏的热力学参数
采用非等温动力学方法研究了聚合物的给氢能力和催化剂在原生煤焦油(PCT)有机质量热破坏过程中的活性。以PCT、磁性微球、镀镍温sotile和fe3o4纳米催化剂为初始原料。Рolymers等聚乙烯(PE),聚苯乙烯(PS)和聚乙二醇(PEG)被选择作为氢供体。通过x射线物相分析(XRD)测定了催化剂(镍沉积温sotile)的Mg3[OH]4{Si2O5}和NiO相,透射电镜(TEM)观察到纳米管表面和内部存在高度分散的氧化镍颗粒。温sotile纳米管表面和内部均匀分布着8 ~ 11 nm和30 ~ 37 nm的氧化镍颗粒。在热重分析的基础上,采用积分法和热重曲线拐点法确定了PCT、催化剂和高分子材料混合物的热破坏动力学参数。建立了活化能、速率常数和指前因子随PCT有机质量破坏程度的增加的变化规律。结果表明,聚合物和催化剂的性质对反应速率常数和活化能的取值有显著影响。在催化剂(镍沉积温石棉)存在下,用第一种方法计算得到的煤焦油- PS和PE混合物的热破坏活化能分别为47.6 kJ/mol和40.4 kJ/mol,用第二种方法计算得到的活化能分别为47.3 kJ/mol和86.5kJ/mol。
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