Department of Chemistry, University of Saskatchewan, 110 Science Place, Saskatoon, Saskatchewan, S7N 5C9, Canada.
Phys Chem Chem Phys. 2011 Jan 21;13(3):1112-22. doi: 10.1039/c0cp00421a. Epub 2010 Nov 12.
The sorption characteristics of naphthenic acids (NAs) in their anion form with β-cyclodextrin (β-CD) based polyurethanes, as sorbents, from aqueous solutions that simulate the conditions of oil sands process water (OSPW) are presented. The copolymer sorbents were synthesized at various β-CD:diisocyanate monomer mole ratios (e.g., 1:1, 1:2, and 1:3) with diisocyanates of variable molecular size and degree of unsaturation. The equilibrium sorption properties of the copolymer sorbents were characterized using sorption isotherms in aqueous solution at pH 9.00 with electrospray ionization mass spectrometry to monitor the equilibrium unbound fraction of anionic NAs in the aqueous phase. The copolymer sorbents were characterized in the solid state using (13)C CP-MAS NMR spectroscopy, IR spectroscopy and elemental analysis. The sorption results of the copolymer sorbents with anion forms of NAs in solution were compared with a commercially available carbonaceous standard: granular activated carbon (GAC). The monolayer sorption capacities of the sorbents (Q(m)) were obtained from either the Langmuir or the Sips isotherm model used to characterize the sorption characteristics of each copolymer sorbent. The estimated sorption capacity for GAC was 142 mg NAs per g sorbent whereas the polymeric materials ranged from 0-75 mg NAs per g sorbent over the experimental conditions investigated. In general, significant differences in the sorption capacities between GAC and the copolymer sorbents were related to the differences in the accessible surface areas and pore structure characteristics of the sorbents. The Sips parameter (K(eq)) for GAC and the copolymer materials reveal differences in the relative binding affinity of NAs to the sorbent framework in accordance with the synthetic ratios and the value of Q(m). The diisocyanate linker plays a secondary role in the sorption mechanism, whereas the β-CD macrocycle in the copolymer framework is the main sorption site for NAs because of the formation of inclusion complexes with β-CD.
本文介绍了β-环糊精(β-CD)基聚氨酯作为吸附剂,从模拟油砂工艺用水(OSPW)条件的水溶液中吸附萘酸(NA)阴离子的吸附特性。合成了不同β-CD:二异氰酸酯单体摩尔比(例如 1:1、1:2 和 1:3)的共聚物吸附剂,所用二异氰酸酯的分子量和不饱和度不同。采用电喷雾电离质谱法在 pH 9.00 的水溶液中通过吸附等温线来监测水相中未结合的阴离子 NA 分数,对共聚物吸附剂的平衡吸附特性进行了表征。采用(13)C CP-MAS NMR 光谱、IR 光谱和元素分析对固态共聚物吸附剂进行了表征。将共聚物吸附剂在溶液中与 NA 的阴离子形式的吸附结果与商业可用的碳质标准:颗粒活性炭(GAC)进行了比较。从 Langmuir 或 Sips 等温线模型中获得了吸附剂的单层吸附容量(Q(m)),用于描述每个共聚物吸附剂的吸附特性。GAC 的估计吸附容量为 142mg NA/g 吸附剂,而在研究的实验条件下,聚合物材料的吸附容量范围为 0-75mg NA/g 吸附剂。一般来说,GAC 和共聚物吸附剂之间的吸附容量差异与吸附剂的可及表面积和孔结构特征的差异有关。GAC 和共聚物材料的 Sips 参数(K(eq))表明,根据合成比和 Q(m)的值,NA 与吸附剂骨架的相对结合亲和力存在差异。二异氰酸酯连接体在吸附机制中起次要作用,而共聚物骨架中的β-CD 大环是 NA 的主要吸附位点,因为它与β-CD 形成包合络合物。