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Enhanced Adsorptive Removal of Methyl Orange and Methylene Blue from Aqueous Solution by Alkali-Activated Multiwalled Carbon Nanotubes

机译:碱活化多壁碳纳米管增强对水溶液中甲基橙和亚甲基蓝的吸附去除

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An alkali-acitvated method was explored to synthesize activated carbon nanotubes (CNTs-A) with a high specific surface area (SSA), and a large number of mesopores. The resulting CNTs-A were used as an adsorbent material for removal of anionic and cationic dyes in aqueous solutions. Experimental results indicated that CNTs-A have excellent adsorption capacity for methyl orange (149 mg/g) and methylene blue (399 mg/g). Alkali-activation treatment of CNTs increased the SSA and pore volume (PV), and introduced oxygen-containing functional groups on the surface of CNTs-A, which would be beneficial to improving the adsorption affinity of CNTs-A for removal of dyes. Kinetic regression results shown that the adsorption kinetic was more accurately represented by a pseudo second-order model. The overall adsorption process was jointly controlled by external mass transfer and intra-particle diffusion, and intra-particle diffusion played a dominant role. Freundlich isotherm model showed a better fit with adsorption data than Langmuir isotherm model. Adsorption interactions of dyes onto CNTs-A from aqueous solutions were investigated using Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD), and Brunauer-Emmett-Teller (BET) method. The remarkable adsorption capacity of dye onto CNTs-A can be attributed to the multiple adsorption interaction mechanisms (hydrogen bonding, π-π electron-donor-acceptor interactions, electrostatic interactions, mesopore filling) on the CNTs-A. Results of this work are of great significance for environmental applications of activated CNTs as a promising adsorbent nanomaterial for organic pollutants from aqueous solutions.
机译:探索了一种碱法合成具有高比表面积(SSA)和大量中孔的活性碳纳米管(CNTs-A)。所得的CNT-A用作吸附剂材料,用于去除水溶液中的阴离子和阳离子染料。实验结果表明,CNTs-A对甲基橙(149 mg / g)和亚甲基蓝(399 mg / g)具有优异的吸附能力。碳纳米管的碱活化处理增加了SSA和孔体积(PV),并在碳纳米管-A的表面引入了含氧官能团,这将有利于提高碳纳米管-A对染料的吸附亲和力。动力学回归结果表明,吸附动力学由伪二级模型更准确地表示。整个吸附过程由外部传质和颗粒内扩散共同控制,而颗粒内扩散起主要作用。 Freundlich等温线模型显示的吸附数据比Langmuir等温线模型更好。使用傅立叶变换红外(FT-IR)光谱,扫描电子显微镜(SEM),X射线衍射(XRD)和Brunauer-Emmett-Teller(BET)方法研究了染料从水溶液到CNTs-A的吸附相互作用。染料在CNTs-A上的出色吸附能力可以归因于CNTs-A上的多种吸附相互作用机理(氢键,π-π电子-供体-受体相互作用,静电相互作用,中孔填充)。这项工作的结果对于活性碳纳米管作为一种有前途的吸附剂纳米材料用于水溶液中有机污染物的环境应用具有重要意义。

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