Bruzzoniti Maria Concetta, Prelle Ambra, Sarzanini Corrado, Onida Barbara, Fiorilli Sonia, Garrone Edoardo
Dipartimento di Chimica Analitica, Università degli Studi di Torino, Torino, Italy.
J Sep Sci. 2007 Oct;30(15):2414-20. doi: 10.1002/jssc.200700182.
Three samples of SBA-15 functionalised with -(CH(2))(3)COOH groups have been prepared by co-condensation, starting from solutions of TEOS and 4-(triethoxysilyl)butyronitrile, acting as -(CH(2))(3)COOH precursor, of different molar compositions. Materials were characterised by X-ray diffraction, nitrogen adsorption, and FT-IR spectroscopy. The pK(a) and the acidic capacity were measured for all samples by potentiometric titration. The acidic capacity increases with increasing amount of -COOH precursor in the synthesis mixture only up to 10% molar of total alkoxysilane. The value for the pK(a)(4.75) is independent of the acidic capacity of the material. The sample prepared starting from an amount of -COOH precursor equal to 10% molar of total alkoxysilane was chosen to test selective interactions with heavy metals of environmental importance (Ag(+), Cd(2+), Fe(3+), Cu(2+), Zn(2+)) at different pH values and ionic strengths. The significant and selective adsorption exhibited by the material has been exploited in a preliminary cation-exchange chromatographic application showing the possibility of eluting the metal ions at different retention times.
通过共缩合制备了三种用-(CH(2))(3)COOH基团功能化的SBA-15样品,起始原料为不同摩尔组成的TEOS和作为-(CH(2))(3)COOH前体的4-(三乙氧基硅基)丁腈溶液。通过X射线衍射、氮吸附和傅里叶变换红外光谱对材料进行了表征。通过电位滴定法测量了所有样品的pK(a)和酸容量。仅在合成混合物中-COOH前体的量增加至总烷氧基硅烷的10%摩尔之前,酸容量随其增加而增加。pK(a)(4.75)的值与材料的酸容量无关。选择从等于总烷氧基硅烷10%摩尔的-COOH前体的量开始制备的样品,以测试在不同pH值和离子强度下与具有环境重要性的重金属(Ag(+)、Cd(2+)、Fe(3+)、Cu(2+)、Zn(2+))的选择性相互作用。该材料表现出的显著且选择性的吸附已在初步的阳离子交换色谱应用中得到利用,显示了在不同保留时间洗脱金属离子的可能性。