Alrasheedi Muneera, El-Bahy Salah M, El-Sayed Refat, Debbabi Khaled F, Amin Alaa S
Department of Chemistry, College of Science, Qassim University Buraidah 51452 Saudi Arabia.
Department of Chemistry, Turabah University College, Taif University Taif Saudi Arabia.
RSC Adv. 2025 Apr 7;15(14):10862-10872. doi: 10.1039/d5ra00352k. eCollection 2025 Apr 4.
Although modern reported methods, such as AAS, ICP-AES, ICP-MS, have good sensitivity, the high cost of equipment, the need for sophisticated instruments, separation and preconcentration steps and experienced technicians along with lack of precise methods make them cumbersome. Solid phase extraction (SPE) emerges as an attractive technique that reduces solvent consumption, minimizes exposure, shortens extraction time, and lowers disposal costs. Herein, a pioneering methodology for the quantification of minute amounts of silver is introduced, using 2-nitro-6-(thiazol-2-yl-diazenyl)phenol (NTDP) as a complexing agent and Triton X-100 as a nonionic surfactant within a ternary surfactant system at a pH of 5.3. This novel extraction strategy demonstrated selective preconcentration. The enriched solution was subjected to spectrophotometric analysis for the quantification of the analyte. After refining extraction and complexation parameters, a remarkable 250-fold increase in the enrichment factor was attained, highlighting a sensitivity boost of 509 times compared with traditional extraction approaches relying solely on nonionic surfactants. The key parameters of molar absorptivity and Sandell sensitivity were determined to be 6.04 × 10 L mol cm and 0.0018 ng cm, respectively. The calibration plot was observed from 5.0-175 ng mL, whereas Ringbom optimum concentrations ranged from 15-160 ng mL. The detection and quantification limits were 1.63 and 4.95 ng mL, respectively. The relative standard deviation (RSD) of the complex was 2.27. The suggested method was efficiently utilized for assessing the Ag concentration in real samples, producing acceptable outcomes.
尽管现代报道的方法,如原子吸收光谱法(AAS)、电感耦合等离子体发射光谱法(ICP - AES)、电感耦合等离子体质谱法(ICP - MS),具有良好的灵敏度,但设备成本高、需要精密仪器、分离和预浓缩步骤以及经验丰富的技术人员,再加上缺乏精确的方法,使得它们使用起来很麻烦。固相萃取(SPE)作为一种有吸引力的技术应运而生,它减少了溶剂消耗,最大限度地减少了暴露,缩短了萃取时间,并降低了处理成本。在此,介绍了一种用于定量微量银的开创性方法,该方法在pH为5.3的三元表面活性剂体系中,使用2 - 硝基 - 6 - (噻唑 - 2 - 基 - 重氮基)苯酚(NTDP)作为络合剂,Triton X - 100作为非离子表面活性剂。这种新颖的萃取策略显示出选择性预浓缩。对富集后的溶液进行分光光度分析以定量分析物。在优化萃取和络合参数后,富集因子显著提高了250倍,与仅依靠非离子表面活性剂的传统萃取方法相比,灵敏度提高了509倍。摩尔吸光系数和桑德尔灵敏度的关键参数分别确定为6.04×10⁴ L·mol⁻¹·cm⁻¹和0.0018 ng·cm⁻²。校准曲线在5.0 - 175 ng·mL⁻¹范围内观察到,而林邦最佳浓度范围为15 - 160 ng·mL⁻¹。检测限和定量限分别为1.63和4.95 ng·mL⁻¹。该络合物的相对标准偏差(RSD)为2.27。所建议的方法有效地用于评估实际样品中的银浓度,产生了可接受的结果。