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Differentiation of adsorption capacity towards selected heavy metal ions throughout oxidised activated carbon granule

机译:在氧化活性炭颗粒中朝向所选重金属离子的吸附能力的分化

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Commercial granulated activated carbon Norit R3ex after demineralisation with conc. HF and HCl acids was oxidised usig conc. nitric acid at 353 K for 3 hrs and heated in vacuum at 423 K. From the oxidised using conc. nitric acid at 353 K for 3 hrs and heated in vacuum at 423 K. From the oxidised carbon the appropriate powdered and core samples were obtained by the method in which the successive layers are removed from the granules by abrasion in a spouted bed. The abrasion treatment was carried out in two steps: elimination of about 33percent and 67percentwt. of the starting granules. The powdered samples were taken from the external and middle layer of the granules leaving behind granular core samples. In all carbon samples total oxygen contents, as well as surface functional oxygen groups were determined. Additionally the surface chemical structure of the samples was determined by FTIR spectroscopy. The excess adsorption isotherms of the selected cations (Fe~(3+), Co~(2+), Cu~(2+)) on the obtained samples were determined at 298 K. Adsorption took place from aqueous solution with different pHs of corresponding nitrates. The relationship between the adsorption capacity and chemical structure of adsorbent surface was analysed and discussed.
机译:用浓度脱落后商业粒状活性炭诺芮特R3ex。 HF和HCl酸被氧化USIG浓度。硝酸在353k,3小时,并在423k真空中加热。从氧化使用浓度。在353k的硝酸对于3小时,在423k的真空中在423k中加热。通过通过磨损在喷射的床中从颗粒中从颗粒中除去连续层的方法获得适当的粉末和核样品。磨损处理分两步进行:消除约33%和67percentwt。起始颗粒。从颗粒的外层和中间层取出留下颗粒核心样品的粉末样品。在所有碳样品中,确定了表面官能氧的总氧含量。另外,样品的表面化学结构由FTIR光谱法测定。在得到的样品上的所选阳离子(Fe〜(3+),Co〜(2+),Cu〜(2+)的过量吸附等温线在298k中测定。吸附从具有不同pH的水溶液相应的硝酸盐。分析并讨论吸附剂表面的吸附能力和化学结构之间的关系。

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