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A comparison between determination of trace amounts of sulfide in the presence and absence of micelle particles in natural waters (Qazvin, Iran): a kinetic spectrophotometric approach

机译:在天然水中存在和不存在胶束颗粒的情况下测定痕量硫化物之间的比较(伊朗加兹温):动力学分光光度法

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A new sensitive kinetic spectrophotometric method described for the determination of trace amounts of sulfides based on the addition reaction of sulfide ions with malachite green has been investigated in aqueous and micellar media at 25 degrees C. The variables affecting the rate of the reaction were investigated, and the optimum conditions were established. Under the optimum experimental conditions, decreases in the absorbance of malachite green at 615 nm in the absence and 630 nm in the presence of micelle particles, their lambda(max), were proportional to the concentrations of sulfide ions at the first 15 and 25 s from initiation of the reaction. The working curve was linear over the concentration range 501200 ng mL(-1) of sulfide ions with a fixed time method at the first 15 and 25 s from initiation of the reaction in aqueous medium and 25-1750 ng mL(-1) with a fixed time method at the first 15 s and 25-1500 ng mL(-1) for primitive 25 s in micellar medium. For the proposed kinetic method, the experimental and theoretical limit of detection (LOD) and limit of quantification (LOQ) in the presence and absence of micelle particles were obtained and tabulated at Delta t=15 and 25 s. The effective range concentration was achieved from the plot of Ringbom in both media and reported. Different surfactants, such as nonionic surfactant (Triton-X100), anionic surfactant sodium dodecyl sulfate (SDS), and cationic surfactant cetyltrimethylammonium bromide (CTAB) and cetylpyridinium chloride (CPC), were investigated and Triton X-100 selected as a suitable surfactant. To valuable vision into the reaction pathways, pseudo-first-order condition was applied and different kinetic parameters like Delta G(not equal), Delta E-not equal, Delta S-not equal, and Delta H-not equal computed. The 2:1 stoichiometry of malachite green to sulfide ions was indicated by the results of mole ratio and Job's method of continuous variation. The effect of different environments on the interfering of various ions on sulfide determination with the suggested method was studied, and final results have been presented. To investigate the usefulness of the different media of the proposed method, sulfide ions were determined in natural waters such as river and spring samples without any purification or using masking reagents.
机译:已经研究了一种新的灵敏的动力学分光光度法,该方法用于在25°C的水和胶束介质中基于硫化物离子与孔雀石绿的加成反应测定痕量硫化物,研究了影响反应速率的变量,并确定了最佳条件。在最佳实验条件下,在无胶束存在的情况下,孔雀石绿在615 nm处的吸光度降低;在存在胶束颗粒的情况下,在630 nm下的吸光度降低,其lambda(max)与前15和25 s时的硫化物离子浓度成正比。从反应开始在开始于水介质中反应开始的前15和25 s的固定时间方法中,在501200 ng mL(-1)的硫化物离子浓度范围内,工作曲线是线性的,在25-1750 ng mL(-1)的条件下,工作曲线是线性的。胶束培养基中原始25 s的最初15 s和25-1500 ng mL(-1)的固定时间方法。对于拟议的动力学方法,在存在和不存在胶束粒子的情况下,获得了实验和理论上的检测极限(LOD)和定量极限(LOQ),并在Delta t = 15和25 s处制成表格。有效范围浓度是从Ringbom在两种介质中的曲线图得出的,并已报道。研究了不同的表面活性剂,例如非离子表面活性剂(Triton-X100),阴离子表面活性剂十二烷基硫酸钠(SDS)和阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)和十六烷基氯化吡啶鎓(CPC),并选择了Triton X-100作为合适的表面活性剂。为了对反应路径有价值,应用了伪一阶条件,并计算了不同的动力学参数,例如Delta G(不相等),Delta E(不相等),Delta S(不相等)和Delta H(不相等)。孔雀绿与硫化物离子的化学计量比为2:1,这是由摩尔比和连续变化的Job方法得出的。研究了所建议的方法对不同环境对各种离子的干扰对硫化物测定的影响,并给出了最终结果。为了研究所提出方法的不同介质的有用性,无需进行任何纯化或使用掩蔽试剂即可在天然水(如河流和春季样品)中测定硫化物离子。

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