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Combination of 13C/113Cd NMR, potentiometry, and voltammetry in characterizing the interactions between Cd and two models of the main components of soil organic matter

机译:结合13 C / 113 Cd NMR,电位法和伏安法表征Cd与两种土壤有机质主要成分模型之间的相互作用

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This work allowed the characterization of the Cd-binding sites of two compounds taken as models for exudates, the main components of soil organic matter (SOM). The studied compounds were exopolysaccharides (EPS), specifically exudates of roots (polygalacturonic acid) and of soil bacteria (Phytagel). Potentiometric acid–base titrations were performed and fitting of the obtained results indicated the presence of two main classes of acidic sites, defined by their pK a values, for both EPS but of a different nature when comparing the two compounds. The two studied exopolysaccharides presented different acidic/basic site ratios: 0.15 for Phytagel and 0.76 for polygalacturonic acid. Spectroscopic techniques (13C/113Cd NMR, FTIR) distinguished different Cd surroundings for each of the studied EPS, which is in agreement with the titration results. Furthermore, these analyses indicated the presence of –COOH and –OH groups in various proportions for each exopolysaccharide, which should be linked to their reactivity towards cadmium. Cadmium titrations (voltammetric measurements) also differentiated different binding sites for each compound and allowed the determination of the strength of the Cd-binding site of the EPS. Fitting of the results of such voltammetric measurements was performed using PROSECE (Programme d’Optimisation et de Speciation Chimique dans l’Environnement), a software coupling chemical speciation calculation and binding parameter optimization. The fitting, taking into account the Cd2+/H+ competition towards exopolysaccharides, confirmed the acid-base titrations and spectroscopic analyses by revealing two classes of binding sites: (i) one defined as a strong complexant regarding its Cd2+–EPS association (logK = 9–10.4) and with basic functionality regarding H+–EPS association (pK a = 11.3–11.7), and (ii) one defined as a weak complexant (logK = 7.1–8.2) and with acidic functionality (pK a = 3.7–4.0). Therefore the combination of spectroscopic analyses, voltammetry, and fitting allowed the precise characterization of the binding sites of the studied exopolysaccharides, mimicking the main SOM components. Furthermore, the binding parameters obtained by fitting can be used in biogeochemical models to better define the role of key SOM compounds like exudates of roots and of soil bacteria on trace metal transport or assimilation.
机译:这项工作允许表征两种化合物的Cd结合位点,这些化合物作为渗出物的模型,是土壤有机质(SOM)的主要成分。研究的化合物是胞外多糖(EPS),特别是根部(聚半乳糖醛酸)和土壤细菌(Phytagel)的渗出液。进行了电位酸碱滴定,对得到的结果进行拟合,结果表明两种EPS都有两种主要的酸性位点,由它们的pK a 值定义,但是在比较这两种化合物时性质不同。两种研究的胞外多糖表现出不同的酸性/碱性位点比率:Phytagel为0.15,聚半乳糖醛酸为0.76。光谱技术(13 C / 113 Cd NMR,FTIR)区分了每种所研究EPS的不同Cd环境,这与滴定结果相符。此外,这些分析表明,每种胞外多糖均以不同比例存在–COOH和–OH基团,这应与它们对镉的反应性有关。镉滴定(伏安法测量)还区分了每种化合物的不同结合位点,并可以确定EPS的Cd结合位点的强度。伏安测量结果的拟合是使用PROSECE(程序优化和特殊化化学环境)进行的,该软件结合了化学形态计算和结合参数优化。考虑到Cd2 + / H + 与胞外多糖的竞争,这种拟合通过揭示两类结合位点证实了酸碱滴定和光谱分析:(i)一种结合位点被定义为强络合剂Cd2 + -EPS关联(logK = 9-10.4),具有有关H + -EPS关联的基本功能(pK a = 11.3-11.7),并且(ii)一种定义为弱(logK = 7.1–8.2)和酸性功能(pK a = 3.7–4.0)。因此,光谱分析,伏安法和拟合的组合可以精确表征所研究胞外多糖的结合位点,从而模仿了主要的SOM成分。此外,通过拟合获得的结合参数可用于生物地球化学模型中,以更好地定义关键SOM化合物(如根和土壤细菌的渗出物)对痕量金属迁移或同化的作用。

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