Asymmetrical flow field flow fractionation -: Multidetection system as a tool for studying metal-alginate interactions

被引:20
作者
Alasonati, Enrica
Stolpe, Bjorn
Benincasa, Maria-Anna
Hassellov, Martin
Slaveykova, Vera I. [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Environm Sci & Technol, Sch Architecture & Civil Engn, CH-1015 Lausanne, Switzerland
[2] Univ Gothenburg, Dept Chem Analyt & Marine Chem, SE-41296 Gothenburg, Sweden
[3] Univ Roma La Sapienza, Dept Chem, I-00185 Rome, Italy
关键词
acidic polysaccharides; biological monitoring; bound residues; FlFFF [flow field flow fractionation; size and molar mass distributions;
D O I
10.1071/EN06024
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The present study explores the potential use of asymmetrical flow field flow fractionation (aFlFFF) with a multidetection system for the study of metal-alginate interactions. aFlFFF, coupled on-line to a differential refractive index and seven angle laser light scattering detectors was used to provide information on the alginate size distributions. In parallel, the metal distributions of metal-alginate complexes were probed by aFlFFF-high resolution inductively coupled plasma-mass spectrometry. Average values and continuous distributions of molar masses, radiuses of gyration and hydrodynamic radiuses, which are critical for understanding the role of alginates as carriers of metal pollutants, were evaluated in presence of Pb or Cd and compared with those in metal-free solutions of alginate. The values of number average and weight average molar mass, weight average radius of gyration and shape factor for alginate were 150 and 188 kg mol(-1), 53 nm and 1.7, respectively. Alginate molar mass and radius of gyration distributions were slightly shifted to higher values by the addition of micromolar concentrations of Pb or Cd. The alginate size distribution in the presence of Cd was similar to the alginate-alone control, whereas in the presence of Pb the size distribution was broader with a shift of the maximum toward higher molar masses.
引用
收藏
页码:192 / 198
页数:7
相关论文
共 42 条
[1]   A major biopolymeric component to dissolved organic carbon in surface sea water [J].
Aluwihare, LI ;
Repeta, DJ ;
Chen, RF .
NATURE, 1997, 387 (6629) :166-169
[2]   Flow field-flow fractionation and characterization of ionic and neutral polysaccharides of vegetable and microbial origin [J].
Benincasa, MA ;
Cartoni, G ;
Delle Fratte, C .
JOURNAL OF CHROMATOGRAPHY A, 2002, 967 (02) :219-234
[3]   A generalized description of aquatic colloidal interactions: The three-colloidal component approach [J].
Buffle, J ;
Wilkinson, KJ ;
Stoll, S ;
Filella, M ;
Zhang, JW .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (19) :2887-2899
[4]   CHARACTERIZATION OF AQUATIC COLLOIDS AND MACROMOLECULES .1. STRUCTURE AND BEHAVIOR OF COLLOIDAL MATERIAL [J].
BUFFLE, J ;
LEPPARD, GG .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (09) :2169-2175
[5]   CHARACTERIZATION OF AQUATIC COLLOIDS AND MACROMOLECULES .2. KEY ROLE OF PHYSICAL STRUCTURES ON ANALYTICAL RESULTS [J].
BUFFLE, J ;
LEPPARD, GG .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (09) :2176-2184
[6]  
Buffle J., 1988, Complexation Reactions in Aquatic Systems
[7]   A log-normal distribution model for the molecular weight of aquatic fulvic acids [J].
Cabaniss, SE ;
Zhou, QH ;
Maurice, PA ;
Chin, YP ;
Aiken, GR .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (06) :1103-1109
[8]   Spontaneous assembly of marine dissolved organic matter into polymer gels [J].
Chin, WC ;
Orellana, MV ;
Verdugo, P .
NATURE, 1998, 391 (6667) :568-572
[9]   Binding of pyrene to aquatic and commercial humic substances: The role of molecular weight and aromaticity [J].
Chin, YP ;
Aiken, GR ;
Danielsen, KM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (06) :1630-1635
[10]   Relating ion binding by fulvic and humic acids to chemical composition and molecular size. 1. Proton binding [J].
Christl, I ;
Kretzschmar, R .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (12) :2505-2511