中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Adsorption behavior of Cu2+ from aqueous solutions onto starch-g-poly(acrylic acid)/sodium humate hydrogels

文献类型:期刊论文

作者Zheng YA(郑易安); Wang AQ(王爱勤)
刊名Desalination
出版日期2010
卷号263期号:1-3页码:170-175
关键词Starch Sodium humate Hydrogel Cu2+ adsorption Complexation
ISSN号0011-9164
通讯作者王爱勤 aqwang@licp.cas.cn
中文摘要A series of starch-g-poly(acrylic acid)/sodium humate (St-g-PAA/SH) hydrogels were prepared and used to adsorb Cu2+ from the aqueous solution. The batch adsorption experiments were carried out by varying contact times (0–90 min), initial Cu2+ concentration (0.003–0.02 mol/L), and pH values (2.0–5.0). The effects of ion strength (5, 10 mmol/L NaCl) and competitive ion (5, 10 mmol/L Pb(NO3)2) on the adsorption capacity were investigated. The results indicated that the addition of 5% SH into St-g-PAA polymeric networks could not only improve the initial adsorption rate and final adsorption capacity for Cu2+, but also make a remarkable contribution to regeneration ability. St-g-PAA/SH hydrogels exhibited high adsorption capacity within a wide pH range and the adsorption data could be well described by the pseudo-second order kinetic model and Langmuir isotherm model. FTIR spectra before and after adsorption of Cu2+ on the hydrogels revealed that complexation was considered as the main adsorption mechanism.
学科主题功能高分子
收录类别SCI
资助信息甘肃省科技厅科技支撑项目(0804GKCA03A)
语种英语
公开日期2012-09-02
源URL[http://210.77.64.217/handle/362003/120]  
专题兰州化学物理研究所_环境材料与生态化学研究发展中心
推荐引用方式
GB/T 7714
Zheng YA,Wang AQ. Adsorption behavior of Cu2+ from aqueous solutions onto starch-g-poly(acrylic acid)/sodium humate hydrogels[J]. Desalination,2010,263(1-3):170-175.
APA 郑易安,&王爱勤.(2010).Adsorption behavior of Cu2+ from aqueous solutions onto starch-g-poly(acrylic acid)/sodium humate hydrogels.Desalination,263(1-3),170-175.
MLA 郑易安,et al."Adsorption behavior of Cu2+ from aqueous solutions onto starch-g-poly(acrylic acid)/sodium humate hydrogels".Desalination 263.1-3(2010):170-175.

入库方式: OAI收割

来源:兰州化学物理研究所

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