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Measurement of the adsorptive capacity of a powder

机译:粉末吸附能力的测量

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The purpose of this work was to recommend a method of measuring the adsorptive capacity of powdered activated carbon(PAC).The adsorptive capacity is needed in future mathematical models of dispersed phase adsorption.This measurement was difficult,because the large drag forces in powders resist any flow into the sample volume,causing big pressure gradients.Two approaches were tested and compared; a material balance over a packed bed,and a standard volumetric method.The pressure loss across the packed bed was made small by the combination of the PAC with glass ballotini.Toluene was chosen as a sorbate because of its ease of measurement.The results concerned pressure variations in the packed bed,and the ease with which the end-points could be found in either method.With regard to the packed bed,the time from the start of breakthrough to saturation was typically 110 min.The principal reason for this delay was channelling; the breakthrough curve could not be used to infer pore diffusion coefficients.The total pressure within the bed was kept to within 5% of its mean value.Hence,the adsorptive capacity could be plotted as a function of pressure,and fitted with a Freundlich isotherm with an exponent of "=0.2.Including the PAC,the adsorptive capacities of four kinds of carbon,at the same temperature and pressure,varied from 8 to 16%.For the volumetric method,at least 3 h were needed for the sorbent and sorbate to reach equilibrium.A mathematical model showed that the uptake curve was controlled by heat transfer.Because the test volume was under a partial vacuum,the technician had to be careful that no air leaked into it during the test.The volumetric method was faster with 250 mu m diameter carbon granules; the end-point was evident after 20 min.In conclusion,a method involving a packed bed was developed to measure the adsorptive capacity of a powder.The end-point was determined easily; the end-point for the volumetric method was indistinct.
机译:这项工作的目的是推荐一种测量粉末状活性炭(PAC)吸附能力的方法。在未来的分散相吸附数学模型中,吸附能力是必需的。由于粉末阻剂中的大阻力,这种测量很困难两种方法均经过测试和比较;填充床的物料平衡和标准的体积法。通过PAC和玻璃巴洛蒂尼的组合,使填充床上的压力损失较小。由于甲苯易于测量,因此选择甲苯作为吸附剂。填充床中的压力变化以及在这两种方法中都能轻松找到终点。对于填充床,从突破开始到饱和的时间通常为110分钟。造成这种延迟的主要原因在窜床内的总压力保持在其平均值的5%以内。因此,可以将吸附容量绘制为压力的函数,并配备Freundlich等温线指数为“ = 0.2”,包括PAC,在相同的温度和压力下,四种碳的吸附能力从8%到16%不等。对于体积法,吸附剂和吸附剂至少需要3 h的吸附时间。数学模型表明吸收曲线受传热控制。由于测试体积处于部分真空状态,技术人员必须小心,不要在测试过程中漏气。体积法速度更快最后,开发了一种使用填充床测量粉末吸附能力的方法,该方法可测定直径为250μm的碳颗粒;终点在20分钟后可见。向前体积法不清楚。

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