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Preparation of activated carbon from lotus stalks with the mixture of phosphoric acid and pentaerythritol impregnation and its application for Ni(II) sorption

机译:磷酸季戊四醇浸渍混合莲花茎制备活性炭及其在镍(Ⅱ)吸附中的应用。

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Activated carbons were prepared from lotus stalks impregnated with H3PO4 solution or the H3PO4 solution mixed with pentaerythritol (PER), producing AC and AC-PER. The results of thermogravimetric analysis and SEM suggested that PER enhanced the depolymerization of lignocelluloses and the degree of cross-linked structure in activation process. The physicochemical properties of AC and AC-PER were characterized by N2 adsorption/desorption, Boehm's titration, Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). AC exhibited much higher values of the BET surface area (1418.78 m~2/g) and total pore volume (1.253 cm~3/g) than that of AC-PER (342.67 cm~2/g and 0.273 cm~3/g). Nevertheless, the results of FTIR, Boehm's titration and XPS showed that AC-PER contained much more surface oxygen-containing functional groups. The sorption equilibrium data for Ni(II) sorption onto the carbons agreed well with the Langmuir model. The maximum sorption capacity derived from Langmuir model was 0.5800 mmol/g for AC and 0.9184 mmol/g for AC-PER (I = 0 mM). Based on the results of sorption studies, FTIR and XPS analysis, several possible mechanisms for these sorption systems were elaborated further. Cation exchange, electrostatic attraction and surface complexation were likely important mechanisms for Ni(II) sorption onto the carbons.
机译:活性炭由浸渍有H3PO4溶液或混合有季戊四醇(PER)的H3PO4溶液的莲lotus制备而成,产生AC和AC-PER。热重分析和扫描电镜的结果表明,PER在活化过程中促进了木质纤维素的解聚和交联结构的程度。 AC和AC-PER的理化性质通过N2吸附/解吸,Boehm滴定,傅立叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)进行表征。 AC的BET表面积(1418.78 m〜2 / g)和总孔体积(1.253 cm〜3 / g)比AC-PER(342.67 cm〜2 / g和0.273 cm〜3 / g)高得多)。然而,FTIR,Boehm滴定法和XPS的结果表明AC-PER含有更多的表面含氧官能团。 Ni(II)吸附到碳上的吸附平衡数据与Langmuir模型非常吻合。从Langmuir模型得出的最大吸附容量对AC为0.5800 mmol / g,对于AC-PER(I = 0 mM)为0.9184 mmol / g。根据吸附研究,FTIR和XPS分析的结果,进一步阐述了这些吸附系统的几种可能机理。阳离子交换,静电吸引和表面络合可能是Ni(II)吸附到碳上的重要机制。

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