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Chemical regeneration mechanism of Fe-impregnated chitosan using ferric chloride

机译:铁氯化铁丙氨酸的化学再生机理

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摘要

A process for the regeneration of spent Fe-impregnated chitosan (Fe-CTS) by continuous fluoride adsorption and chemical regeneration is described. Different concentrations of NaCl, FeCl3 and CaCl2 solutions were employed as regenerants. The regeneration efficiencies were valued using 100 mg L-1 fluoride adsorption on regenerated Fe-CTS. Results showed that the maximum adsorption capacity (q(e)) of 14.44 mg g(-1) was obtained when the Fe3+ regenerant concentration was 150 mg L-1. Changes in F- and Cl- concentration were also measured. To examine the stability of regenerated Fe-CTS, Fe3+ leaching was observed in the fluoride solution after adsorption. Scanning electron microscopy with an electronic differential system and surface charge distribution were performed to elucidate the regeneration and adsorption mechanisms. Holes and cracks that emerged after regeneration accelerated the rate of internal diffusion. After regeneration, the FeCl3 solution pH was less than pHpzc (4.92), indicating that FeCl3 regenerated Fe-CTS (FeCl3-Fe-CTS) was positively charged. The change in the concentration of fluoride was consistently greater than that of chloride, indicating that other mechanisms except ion-exchange, such as electrostatic attraction, contributed to fluoride adsorption. After seven regeneration/adsorption cycles, the total adsorption capacity of FeCl3-Fe-CTS was found to be 74.04 mg g(-1) without a significant loss in the adsorption ability.
机译:描述了通过连续氟化物吸附和化学再生进行废Fe-Imperated壳聚糖(Fe-CTS)的再生方法。使用不同浓度的NaCl,FECL3和CaCl 2溶液作为再生剂。在再生Fe-CTS上使用100mg L-1氟化物吸附来重视再生效率。结果表明,当Fe3 +再生浓度为150mg L-1时,获得14.44mg G(-1)的最大吸附容量(Q(e))。还测量了F-和CL-浓度的变化。为了检查再生Fe-CTS的稳定性,在吸附后在氟化物溶液中观察到Fe3 +浸出。进行扫描电子微分系统和表面电荷分布以阐明再生和吸附机制。再生后出现的孔和裂缝加速了内部扩散速率。再生后,FECL3溶液pH小于PHPZC(4.92),表明FECL3再生Fe-CTS(FECL3-FE-CTS)被带正电荷。氟化物浓度的变化始终大于氯化物的变化,表明除离子交换之外的其他机制如静电吸附,有助于氟化物吸附。经过七次再生/吸附循环后,发现FECL3-Fe-CTS的总吸附能力为74.04mg(-1),无需吸附能力显着损失。

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  • 来源
    《RSC Advances》 |2015年第95期|共9页
  • 作者单位

    China Univ Geosci Sch Water Resources &

    Environm Beijing 100083 Peoples R China;

    China Univ Geosci Sch Water Resources &

    Environm Beijing 100083 Peoples R China;

    China Univ Geosci Sch Water Resources &

    Environm Beijing 100083 Peoples R China;

    Tsinghua Univ Sch Environm Beijing 100084 Peoples R China;

    China Univ Geosci Sch Water Resources &

    Environm Beijing 100083 Peoples R China;

    China Univ Geosci Sch Water Resources &

    Environm Beijing 100083 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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