Dynamics of boric acid sorption by boron-selective SB-type anionite

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Abstract

Investigation and choice of an effective sorbent are significant for protection of water bodies against boron The boron high concentration in natural waters produces toxic impact on aquatic biota due to its high biological activity. This paper studied the dynamics of boric acid sorption from aqueous solutions by polycondensation anionite SB-1 synthesized on the base of monoethanolamine and epichlorohydrin. The anion exchanger contained aminooxyethyl and alcohol functional groups in its structure. Methods. It has been established the influences of the ion form of the anionite on the dynamic characteristics of boron sorption from both a model boric acid aqueous solution (0.43 mol/dm3) and an industrial wastewater effluent after boric acid production (0.47 mol/dm3), other things being equal (pH = 5.0; the volume rate of the solution passing through the anionite layer = 1.5 ml/min∙cm2; t = 20 0C). Structural studies to determine the form of boron in the anionite phase were performed using the IR spectroscopic method. Dynamic characteristics of boron sorption (the cation and overall ion-exchange capacity values, period of the protecting effect of the filter) were determined graphically from the sorption curves. Results. It has been found that the hydroxyl form of the anion exchanger SB-1, in comparison with the chlorine form, performs superequivalent boron sorption while boron sorption from both a model and real production solutions. For the first time we have demonstrated that at the initial stage, boric acid sorption is carried out owing to the chemisorption, resulting to the formation of stable hydroxoborate forms [B(OH)4]– in the ionite phase. As the anionite is being saturated and the concentration of free functional hydroxyl groups is decreasing, the formation of polynuclear forms of boric acid [B4O5(OH)4]2– occurs in the anionite phase by sorption of boric acid molecules on free tetrahydroxoborate anions and, further, the complex formation of polynuclear forms of boron by the nitrogen atom of aminooxyethyl functional groups. It has been stated that desorption of boron from anionite is considered to be effective when carried out with a 2 n. NaOH solution with a regeneration degree of 0.995.
硼选择性sb型阴离子对硼酸的吸附动力学
研究和选择有效的吸附剂对水体防硼具有重要意义。天然水体中高浓度的硼具有较高的生物活性,对水生生物产生毒性影响。研究了以单乙醇胺和环氧氯丙烷为原料合成的缩聚阴离子酸SB-1对硼酸的吸附动力学。阴离子交换剂的结构中含有氨基氧乙基和醇官能团。方法。在其他条件相同(pH = 5.0)的情况下(pH = 5.0;溶液通过阴离子层的体积率= 1.5 ml/min∙cm2;t = 20℃)。利用红外光谱法对阴离子相中硼的形态进行了结构研究。硼吸附的动态特性(阳离子交换容量和总离子交换容量值,过滤器的保护作用周期)由吸附曲线图形确定。结果。研究发现,阴离子交换剂SB-1的羟基形式与氯形式相比,在模型溶液和实际生产溶液中都具有超等效的硼吸附。我们首次证明了在初始阶段,由于化学吸附,硼酸吸附被进行,导致在离子相中形成稳定的羟基硼酸盐形式[B(OH)4] -。随着阴离子的饱和和游离官能团羟基浓度的降低,硼酸分子吸附在游离四羟基硼酸阴离子上形成硼酸[B4O5(OH)4]2 -的多核形式,进一步,氨基氧乙基官能团的氮原子络合形成硼的多核形式。研究表明,在再生度为0.995的2 n NaOH溶液中进行硼的脱附是有效的。
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