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Study of the modification mechanism of heavy metal ions adsorbed by biomass-activated carbon doped with a solid nitrogen source

机译:固氮源掺杂生物质活性炭吸附重金属离子的改性机理研究

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In this study, the N-doping of biomass-activated carbon with dicyandiamide was performed via an ultrasonic method and a redox method. BET, SEM, EDS, FT-IR and XPS were used to determine the pore structures, morphologies and surface chemistry of the adsorbents obtained. The N-doping effect of the two modification methods on the same solid nitrogen source was evaluated and the simulated adsorption experiments of heavy metal ions in wastewater were conducted. The results showed that the N-doped biomass-activated carbon having the higher doping content was obtained by a redox method with nitric acid at 25 °C, a solid nitrogen source ratio of 1?:?1 and charring at 800 °C for 2 hours. The adsorption efficiency for the divalent copper ion of the sample obtained by the redox method was 41.15% higher than that of the ultrasonic method sample, and proved that pyridinium nitrogens and amino groups play important roles in adsorption and complexation processes. The isothermal adsorption experiments of N-doped activated carbon conformed to the Freundlich model, which mainly depended on chemical adsorption. The kinetics for copper ion adsorption followed a pseudo-second-order kinetic model. Thermodynamic experiments showed that a higher temperature was advantageous to adsorption. Simultaneously, this study further analyzed the N-doping process of the redox method sample and suggested that improvements can be implemented in the N-doping of activated carbon with solid nitrogen sources.
机译:在这项研究中,通过超声方法和氧化还原方法对双氰胺进行生物质活性炭的N掺杂。 BET,SEM,EDS,FT-IR和XPS用于确定所获得的吸附剂的孔结构,形态和表面化学性质。评价了两种改性方法对同一固体氮源的氮掺杂效果,并进行了废水中重金属离子的吸附模拟实验。结果表明,采用氧化还原法在25°C的硝酸条件下,固氮源比为1?:?1,在800°C的温度下炭化2,可以得到较高掺杂含量的N掺杂生物质活性炭。小时。氧化还原法获得的样品对二价铜离子的吸附效率比超声法获得的样品高41.15%,证明吡啶鎓氮和氨基在吸附和络合过程中起着重要作用。氮掺杂活性炭的等温吸附实验符合Freundlich模型,其主要依赖于化学吸附。铜离子吸附的动力学遵循伪二级动力学模型。热力学实验表明,较高的温度有利于吸附。同时,本研究进一步分析了氧化还原方法样品的N掺杂过程,并建议可以通过使用固氮源对活性炭进行N掺杂来实现改进。

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