Shen J, Ebner AD, Ritter JA
Swearingen Engineering Center, University of South Carolina, Columbia, South Carolina, 29208
J Colloid Interface Sci. 1999 Jun 15;214(2):333-343. doi: 10.1006/jcis.1999.6206.
A series of magnetic adsorbents (silica-magnetite composite oxides) containing 0, 20, 40, 60, 80, and 100 wt% magnetite were prepared via the sol-gel process, where 0.1-µm-radius magnetite particles were encased in a mesoporous silica matrix. The experimental pHpzc for each of the pure oxides and their mixtures was tested against two applicable models in the literature; neither model explained the observed behavior. One of the models did not account for the heterogeneous nature of the two distinct surfaces present in these silica-magnetite composite oxides, and neither model accounted for the possibility of the silica locally altering the behavior of the magnetite functional groups. The behavior was corroborated independently, however, based on an analysis carried out with the measured surface acidity constants. This work also showed that the total exchange capacity of each of the mixed oxides was dominated by the high surface area of the silica, and that the electrolyte species, Na+ or NO-3, did not completely complex with the surface of the oxides, as expected for weak binding ions. The chemical component of the free energy of adsorption of protons for the acid-base reactions also dominated the solvation and coulombic contributions for each of the pure oxides and their mixtures. Copyright 1999 Academic Press.
通过溶胶 - 凝胶法制备了一系列含有0、20、40、60、80和100 wt%磁铁矿的磁性吸附剂(二氧化硅 - 磁铁矿复合氧化物),其中半径为0.1μm的磁铁矿颗粒被包裹在介孔二氧化硅基质中。针对文献中的两个适用模型测试了每种纯氧化物及其混合物的实验零电荷点pH值;两个模型均无法解释观察到的行为。其中一个模型没有考虑这些二氧化硅 - 磁铁矿复合氧化物中存在的两种不同表面的非均质性,且两个模型都没有考虑二氧化硅局部改变磁铁矿官能团行为的可能性。然而,基于对测量的表面酸度常数进行的分析,该行为得到了独立证实。这项工作还表明,每种混合氧化物的总交换容量由二氧化硅的高比表面积主导,并且电解质物种Na⁺或NO₃⁻并未如弱结合离子预期的那样与氧化物表面完全络合。酸碱反应中质子吸附自由能的化学成分也主导了每种纯氧化物及其混合物的溶剂化和库仑贡献。版权所有1999年学术出版社。