Reversible Metal Ion/Complex Binding to Chitin Controlled by Ligand, Redox, and Photochemical Reactions and Active Movement of Chitin on Aquatic Arthropods

S. Fränzle, Felix Blind
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Abstract

There is strong adsorption of metal ions and their complexes to chitin, which depends on both the oxidation and complexation states of many of the said elements (whereas others display chemical reactions detectable via electrochemical methods while being retained by chitin); thus, ad- and desorption at ambient water concentrations (often in the nMol/L range) are controlled by the presence and photochemical properties (concerning Eu and probably U and Ag) of mainly biogenic organic matter (both DOC and POC, and DON). With chitin forming the outer hull of mobile organisms (animals), this biopolymer is expected to take part in metal distribution in aquatic (limnetic and riverine) ecosystems. Having studied the attachment of many different elements to both crayfish and grafted (marine shrimp) chitin, with the highest accumulations observed in Bi, V, Ni, and LREEs, one should consider secondary biochemical transformations which take place at different water and sediment levels. After chitin had been embedded into sediment, methanogenesis (which requires Ni), Bi, and Sb biomethylations and photodesorption in the illuminated water column will occur if there are appropriate organics, causing the vertical separation of Eu from other REEs, at least during the daytime. Eutrophication will enhance both the production and especially the photooxidation rates of organics in water because phosphorylated sugars and lipids are formed quantitatively within min P, which enter water and undergo Eu-mediated photooxidation much more readily. Another biopolymer, gelatin, acts as an inert matrix-enhancing organic photooxidation product via Eu, producing chemical waves, indicating autocatalysis upon light impact. From the redox-related photodesorption of metal analytes from chitin, both sensors and devices for (light-assisted) electrochemical energy conversion are being developed by our workgroup. The electrochemical determination of adsorption thermodynamics on chitin is thus directly linked to its applications in environmental monitoring and technology.
配体、氧化还原和光化学反应控制的金属离子/配合物与甲壳素的可逆结合以及水生节肢动物甲壳素的主动运动
金属离子及其络合物对几丁质有很强的吸附作用,这取决于许多上述元素的氧化和络合状态(而其他元素则通过电化学方法检测到化学反应,同时被几丁质保留);因此,在环境水浓度(通常在nMol/L范围内)下的吸附和解吸受主要生物源有机物(DOC和POC以及DON)的存在和光化学性质(涉及Eu,可能还有U和Ag)的控制。随着几丁质形成活动生物(动物)的外壳,这种生物聚合物有望在水生(湖泊和河流)生态系统中参与金属分布。在研究了许多不同元素在小龙虾和嫁接(海虾)几丁质上的附着,并在Bi、V、Ni和LREEs中观察到最高的积累后,我们应该考虑在不同的水和沉积物水平下发生的二次生化转化。几丁质嵌入沉积物后,如果存在适当的有机物,则会在光照的水柱中发生甲烷生成(需要Ni)、Bi和Sb的生物甲基化和光解吸,导致Eu与其他稀土元素的垂直分离,至少在白天是这样。富营养化将提高水中有机物的产量,特别是光氧化速率,因为磷酸化糖和脂质在min P内定量形成,它们进入水中并更容易进行eu介导的光氧化。另一种生物聚合物,明胶,作为一种惰性基质增强有机光氧化产物,通过Eu,产生化学波,表明光影响下的自催化作用。从甲壳素中金属分析物的氧化还原相关光解吸,我们的工作组正在开发(光辅助)电化学能量转换的传感器和设备。甲壳素吸附热力学的电化学测定直接关系到甲壳素在环境监测和技术中的应用。
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