摘要
为探讨酿酒酵母与Ag+的相互作用机制,分析了酵母吸附Ag+过程中细胞阳离子的释放状况,并利用红外光谱(FTIR)、带能谱仪的扫描电镜(SEM-EDX)、带能谱仪的透射电镜(TEM-EDX)等手段表征了酵母细胞在吸附Ag+前后表面官能团的变化以及Ag+在酵母细胞中的存在位置和状态.结果表明,酵母细胞吸附Ag+伴随着大量细胞阳离子K+、Na+、Mg2+、Ca2+的释放.Ag+的存在会抑制体系pH值增加,并促进Mg2+、Ca2+的释放.与Ag+的吸附类似,K+、Na+、Mg2+、Ca2+的释放也很快,并且符合准二级动力学方程.酵母对Ag+的吸附,可被认为是离子交换机制和共价结合机制共同发挥作用.FTIR证明酵母表面羧基对Ag+的吸附发挥重要作用.电镜分析结果表明,酵母细胞表面不仅吸附了Ag+,同时产生更高浓度的含Ag沉淀物,使Ag+从溶液中去除,这些含Ag沉淀不均匀地分布于细胞表面,含Ag沉淀的性质以及形成过程还需要借助其他分析手段进行进一步确认.
To understand the characteristics of Ag^+ biosorption by the waste biomass of Saccharomyces cerevisiae, the release phenomena of the cell physiological cations,such as K^+ , Mg^2+ , Ca^2+ , Na^+ , and pH value change during Ag^+ uptake were investigated. The presence of Ag^+ promoted the release of the cations,and decreased the absorption of H^+ .Ion exchange was one of the mechanisms involved in metal-microbe interaction. Ag^+ also exhibited a degree covalent binding with the biomass. Both Ag^+ uptake and cation release (K^+ , Mg^+ , Ca^2+ or Na^+ ) followed the pseudo-second order kinetics. Fourier transform infrared spectroscopy (FTIR) indicated that the carboxyl group on the surface of the cells could play important role in metal-microbe interaction. The scanning electron microscopy with energy-dispersive X-ray analysis (SEM- EDX) and transmission electron microscopy with energy-dispersive X-ray analysis (TEM-EDX) were used to directly observe the change of the component elements and surface configuration of the cells before and after the interaction of the microbe with Ag ^+ , and the results proved that Ag^+ was adsorbed by the cell surface. Simultaneously,the precipitate containing Ag with higher concentration than the surface-adsorbed Ag was formed on the cell surface also resulted in the removal of Ag^+ from the aqueous solution.
出处
《环境科学》
EI
CAS
CSCD
北大核心
2008年第12期3561-3567,共7页
Environmental Science
基金
国家自然科学基金项目(50830302)
国家重点实验室(环境模拟与污染控制国家重点联合实验室)专项基金项目(08K05ESPCT)
中国博士后科学基金项目(20080430350)
关键词
酿酒酵母
生物吸附
AG^+
相互作用
机制
Saccharomyces cerevisiae
biosorption
Ag^+
interaction
mechanism