Bozseki Ayşe, İmamoğlu Mustafa, Avcı Davut, Atalay Yusuf
Sakarya University, Science Faculty, Chemistry Department, 54187 Sakarya Türkiye.
Sakarya University, Science Faculty, Chemistry Department, 54187 Sakarya Türkiye.
J Chromatogr A. 2025 Aug 30;1757:466118. doi: 10.1016/j.chroma.2025.466118. Epub 2025 Jun 4.
In the present study, a new chelating sorbent was created by covalently attaching N-((6-(2-thienyl)pyridin-2-yl)methyl)propan-1-amine to the surface of silica (THIOPAM-SG). The sorbent structure was confirmed by C, H, N, S elemental analysis and FT-IR spectroscopy, and subsequently used for the column solid-phase extraction (SPE) of Pd(II) and Au(III) from environmental waters for their accurate and sensitive quantification using flame atomic absorption spectrometry. Key parameters influencing the extraction of Pd(II) and Au(III) was studied. The material demonstrated excellent adsorptive performance towards Pd(II) and Au(III) ions under acidic conditions (0.1 M HCl) at a high sample flow rate of 7.5 mL/min. The retained analytes on the SPE column were easily stripped using 3.0% thiourea in 1.0 M HCl (10 mL) at sample flow rate of 2.5 mL/min. The THIOPAM demonstrated the ability to collect collect trace level of Pd(II) and Au(III) ions from large volume of aqueous samples providing a enrichment factor of 50. The detection limits (3σ) of the developed method for Pd(II) and Au(III) ions were computed to be 1.04 µg/L and 0.38 µg/L, respectively. By the determination of Pd(II) and Au(III) ions at 0.4 mg/L, the quantitative recoveries (≥95%) and low RSD values (≤2.0%) were obtained. The uptake capacity of THIOPAM for Au(III) and Pd(II) ions was figured out to be 52.1 mg/g and 51.2 mg/g, respectively. The proposed novel SPE method was effectively used to quantify Pd(II) and Au(III) trace-level concentrations in various environmental water samples, such as tap, sea, river, and deionized waters. Furthermore, the DFT/HSEh1PBE/LanL2DZ method was applied to determine the coordination environment and interactions between Pd(II) and Au(III) with THIOPAM, as well as to investigate the frontier molecular orbital surfaces and energies and chemical reactivity parameters.
在本研究中,通过将N-((6-(2-噻吩基)吡啶-2-基)甲基)丙-1-胺共价连接到硅胶表面,制备了一种新型螯合吸附剂(THIOPAM-SG)。通过C、H、N、S元素分析和傅里叶变换红外光谱对吸附剂结构进行了确认,随后将其用于环境水样中Pd(II)和Au(III)的柱固相萃取(SPE),以便使用火焰原子吸收光谱法对其进行准确、灵敏的定量分析。研究了影响Pd(II)和Au(III)萃取的关键参数。该材料在酸性条件(0.1 M HCl)下,以7.5 mL/min的高样品流速,对Pd(II)和Au(III)离子表现出优异的吸附性能。在2.5 mL/min的样品流速下,使用1.0 M HCl(10 mL)中的3.0%硫脲可轻松洗脱SPE柱上保留的分析物。THIOPAM能够从大量水样中收集痕量水平的Pd(II)和Au(III)离子,富集因子为50。所开发方法对Pd(II)和Au(III)离子的检测限(3σ)分别计算为1.04 µg/L和0.38 µg/L。通过测定0.4 mg/L的Pd(II)和Au(III)离子,获得了定量回收率(≥95%)和低相对标准偏差值(≤2.0%)。THIOPAM对Au(III)和Pd(II)离子的吸附容量分别为52.1 mg/g和51.2 mg/g。所提出的新型SPE方法有效地用于定量分析各种环境水样(如自来水、海水、河水和去离子水)中痕量水平的Pd(II)和Au(III)浓度。此外,采用密度泛函理论/混合杂化交换泛函/LanL2DZ方法确定Pd(II)和Au(III)与THIOPAM之间的配位环境和相互作用,以及研究前线分子轨道表面、能量和化学反应性参数。