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使用化学力滴定法研究苯甲酸和磷酸盐与氧化铁胶体的相互作用。

Interactions of benzoic acid and phosphates with iron oxide colloids using chemical force titration.

作者信息

Liang Jana, Horton J Hugh

机构信息

Department of Chemistry, Queen's University, Kingston, Ontario, Canada.

出版信息

Langmuir. 2005 Nov 8;21(23):10608-14. doi: 10.1021/la0518290.

Abstract

Colloidal iron oxides are an important component in soil systems and in water treatment processes. Humic-based organic compounds, containing both phenol and benzoate functional groups, are often present in these systems and compete strongly with phosphate species for binding sites on the iron oxide surfaces. Here, we examine the interaction of benzoate and phenolic groups with various iron oxide colloids using atomic force microscopy (AFM) chemical force titration measurements. Self-assembled monolayers (SAMs) of 4-(12-mercaptododecyloxy)benzoic acid and 4-(12-mercaptododecyloxy)phenol were used to prepare chemically modified Au-coated AFM tips, and these were used to probe the surface chemistry of a series of iron oxide colloids. The SAMs formed were also characterized using scanning tunneling microscopy, reflection-absorption infrared spectroscopy, and X-ray photoelectron spectroscopy. The surface pK(a) of 4-(12- mercaptododecyloxy)benzoic acid has been determined to be 4.0 +/- 0.5, and the interaction between the tip and the sample coated with a SAM of this species is dominated by hydrogen bonding. The chemical force titraton profile for an AFM probe coated with 4-(12- mercaptododecyloxy)benzoic acid and a bare iron oxide colloid demonstrates that the benzoic acid function group interacts with all three types of iron oxide sites present on the colloid surface over a wide pH range. Similar experiments were carried out on colloids precipitated in the presence of phosphoric, gallic, and tannic acids. The results are discussed in the context of the competitive binding interactions of solution species present in soils or in water treatment processes.

摘要

胶体氧化铁是土壤系统和水处理过程中的重要组成部分。含有酚和苯甲酸酯官能团的腐殖质基有机化合物通常存在于这些系统中,并与磷酸盐物种在氧化铁表面的结合位点上存在强烈竞争。在此,我们使用原子力显微镜(AFM)化学力滴定测量来研究苯甲酸酯和酚基团与各种氧化铁胶体的相互作用。4-(12-巯基十二烷氧基)苯甲酸和4-(12-巯基十二烷氧基)苯酚的自组装单分子层(SAMs)用于制备化学修饰的金涂层AFM探针,并用于探测一系列氧化铁胶体的表面化学性质。形成的SAMs还使用扫描隧道显微镜、反射吸收红外光谱和X射线光电子能谱进行了表征。已确定4-(12-巯基十二烷氧基)苯甲酸的表面pK(a)为4.0±0.5,并且该物种的SAM涂层尖端与样品之间的相互作用主要由氢键主导。涂有4-(12-巯基十二烷氧基)苯甲酸的AFM探针与裸露的氧化铁胶体的化学力滴定曲线表明,苯甲酸官能团在很宽的pH范围内与胶体表面存在的所有三种类型的氧化铁位点相互作用。对在磷酸、没食子酸和单宁酸存在下沉淀的胶体进行了类似的实验。结果在土壤或水处理过程中存在的溶液物种的竞争结合相互作用的背景下进行了讨论。

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