利用三维荧光光谱(3DEEM)和傅立叶转换红外光谱(FTIR)研究了藻菌生物膜EPS与Al^3+的相互作用机理.3DEEM结果表明,生物膜EPS含有3个荧光峰.其中,峰A(Ex/Em=225~235nm/300-330nm)和峰B(Ex/Em=275-280nm/325~330nm)荧光较强,属类蛋白峰,峰C(Ex/Em=335nm/432~434nm)荧光较弱,属类腐殖酸峰.峰A和峰B都能不同程度地被Al^3+猝灭,它们的条件稳定常数(logK)分别为5.89和6.95.Al^3+-EPS体系的峰A和峰B荧光强度明显受溶液pH值的影响.在pH为2~4之间时,荧光强度随pH的增大而增大,在4-7之间随pH的增大而减小,在7~11之间随pH增大而增大.FTIR光谱图分析表明,Al^3+主要与EPS中所含的-NH-、C=O等发生强的配位作用.
Three-dimensional excitation emission matrix fluorescence spectroscopy (3DEEM) and fourier transform infrared (FTIR) spectroscopy were used to study the extracellular polymeric substances (EPS) produced by alga-bacteria biofilm. Three excitation/emission (Ex/Em) fluorescence peaks at Ex/Em 225-235/300-330 nm (Peak A), 275-280/325-330 nm (Peak B), and 335/432-434 nm (Peak C) were identified in the 3DEEM, respectively. Peaks A and B were referred to as proteinlike fluorescence and peak C as humic-like fluorescence. The fluorescence intensity at both peaks A and B decreased as Al^3+ concentration increased. The values of logK (conditional stability constant) for peaks A and B were 5.89 and 6.95, respectively. It was a/so found that solution pH strongly affected the fluorescence intensity at peaks A and B for the Al^3+-EPS complexation. The fluorescence intensity at peaks A and B increased consistently with solution pH increasing from 2 to 4, decreased with solution pH increasing from 4 to 7, and increased again with solution pH increasing from 7 to 11. FTIR analysis demonstrated that --NH-- and C==O groups in EPS were responsible for binding with Al^3+.