Complexation of magnesium ions in sodium dodecyl benzenesulfonate-Flopaam AN125SH mixtures using sodium citrate

IF 2.6 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Polyhedron Pub Date : 2025-02-01 Epub Date: 2024-12-04 DOI:10.1016/j.poly.2024.117339
Csaba Bús , László Janovák , Ágota Deák , Áron Ágoston , Cora Deák , Ákos Kukovecz , Pál Sipos
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Abstract

Presence of divalent metal ions, especially alkaline earth cations in brine water is an important factor during different processes applying anionic surfactants and negatively charged polymers, because these cations bind to the anionic head group of surfactants and may cause the precipitation of these materials. They also interact with the polymer chains, decreasing the polymer’s viscosity, reducing the net charge of the polymer chains, which also may lead to precipitation. The present study focuses on describing the interactions between magnesium ions with anionic sodium dodecyl benzenesulfonate (SDBS)–Flopaam AN125SH mixtures and the complexation of the magnesium with sodium citrate. Description of these interactions are important to evaluate the applicability of sodium citrate to decrease the undesired effects of alkaline earth cations in polymer-surfactant mixtures. The mixtures contained the high molecular weight anionic polymer in constant 1.0 g/L concentration and the surfactant in 5.0 g/L concentration. The magnesium ion concentration was systematically increased in the samples (0.03–1.5 g/L) and sodium citrate was added to the magnesium ion containing samples in 2.0 and 3.0 M equivalent amount compared to the magnesium ion concentration. The samples were characterized by using turbidimetry and rheology measurements (measuring consistency index, yield stress, flow number and zero shear viscosity), as the change of viscosity is an important parameter during application of polymers in different processes. The formed precipitates were characterized using infrared spectroscopy. The results showed that sodium citrate successfully inhibited the magnesium ions caused precipitation up to 1.2 g/L metal ion concentration (1200 ppm), but caused a considerable decrease in the viscosity of the samples (the consistency index of the mixtures decreased from 47.5 mPa s to 7.53 mPa s) and that magnesium ions do not induce precipitation of the polymer. However, this amount of decrease in viscosity did not change the flow properties of the polymer, all the investigated samples were measured to possess pseudoplastic flow behavior. The viscosity decreasing effects of the sodium citrate were also measured and approximately 13.0 mPa s decrease was measured in zero shear viscosity.

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柠檬酸钠对十二烷基苯磺酸钠-氟帕泮- AN125SH混合物中镁离子的络合作用
在使用阴离子表面活性剂和带负电荷的聚合物的不同过程中,盐水中存在的二价金属离子,特别是碱土阳离子是一个重要因素,因为这些阳离子与表面活性剂的阴离子头基团结合,可能导致这些物质的沉淀。它们还与聚合物链相互作用,降低聚合物的粘度,减少聚合物链的净电荷,这也可能导致沉淀。本研究主要描述了镁离子与阴离子十二烷基苯磺酸钠(SDBS) -Flopaam - AN125SH混合物之间的相互作用以及镁与柠檬酸钠的络合作用。描述这些相互作用对于评价柠檬酸钠在减少碱土阳离子在聚合物-表面活性剂混合物中的不良影响方面的适用性是重要的。混合物中含有1.0 g/L浓度的高分子量阴离子聚合物和5.0 g/L浓度的表面活性剂。系统地提高样品中的镁离子浓度(0.03 ~ 1.5 g/L),并在含镁离子的样品中添加2.0和3.0 M当量的柠檬酸钠,与镁离子浓度比较。由于粘度的变化是聚合物在不同工艺应用过程中的重要参数,因此采用比浊法和流变学测量(测量稠度指数、屈服应力、流动数和零剪切粘度)对样品进行了表征。用红外光谱对形成的析出物进行了表征。结果表明,当金属离子浓度达到1.2 g/L (1200 ppm)时,柠檬酸钠成功地抑制了镁离子的析出,但使样品的黏度显著降低(混合物的稠度指数从47.5 mPa s降至7.53 mPa s),且镁离子不会引起聚合物的析出。然而,这种粘度的降低并没有改变聚合物的流动特性,所有被研究的样品都具有假塑性流动行为。柠檬酸钠的降粘效果也进行了测试,在零剪切粘度下,柠檬酸钠的降粘效果约为13.0 mPa。
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来源期刊
Polyhedron
Polyhedron 化学-晶体学
CiteScore
4.90
自引率
7.70%
发文量
515
审稿时长
2 months
期刊介绍: Polyhedron publishes original, fundamental, experimental and theoretical work of the highest quality in all the major areas of inorganic chemistry. This includes synthetic chemistry, coordination chemistry, organometallic chemistry, bioinorganic chemistry, and solid-state and materials chemistry. Papers should be significant pieces of work, and all new compounds must be appropriately characterized. The inclusion of single-crystal X-ray structural data is strongly encouraged, but papers reporting only the X-ray structure determination of a single compound will usually not be considered. Papers on solid-state or materials chemistry will be expected to have a significant molecular chemistry component (such as the synthesis and characterization of the molecular precursors and/or a systematic study of the use of different precursors or reaction conditions) or demonstrate a cutting-edge application (for example inorganic materials for energy applications). Papers dealing only with stability constants are not considered.
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