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使用单、二和三铵官能化 SBA-15 从水溶液中吸附去除二氢磷酸盐离子。

Adsorptive removal of dihydrogenphosphate ion from aqueous solutions using mono, di- and tri-ammonium-functionalized SBA-15.

机构信息

Department of Soil Sciences & Agri-Food Engineering, Université Laval, Que., Canada G1V 0A6.

出版信息

J Colloid Interface Sci. 2010 Mar 15;343(2):615-21. doi: 10.1016/j.jcis.2009.11.070. Epub 2009 Dec 4.

DOI:10.1016/j.jcis.2009.11.070
PMID:20035944
Abstract

Adsorption of monovalent phosphate anions from aqueous solutions on mono, di- and tri-ammonium-functionalized mesoporous SBA-15 silica was investigated. The adsorbent was prepared via a post-synthesis grafting method, using 3-aminopropyltrimethoxysilane (N-silane), [1-(2-aminoethyl)-3-aminopropyl]trimethoxysilane (NN-silane) and 1-[3-(trimethoxysilyl)-propyl]-diethylenetriamine (NNN-silane), followed by acidification in HCl solution to convert the attached surface amino groups to positively charged ammonium moieties. The loading of amino moieties on the SBA-15 surface was varied from 5% to 40% as organoalkoxysilane/silica molar ratio. The adsorption experiments were conducted batchwise at room temperature. Results showed that adsorption capacity increased with increasing the concentration of functional groups on the SBA-15 adsorbent whatever the nature of the functional group. In the case of monoammonium functional groups, the adsorption capacity increased from 0.64 to 1.07 mmol H(2)PO(4)(-)/g when the molar ratio organoalkoxysilane/silica was varied from 5% to 40%, respectively. Similar tendency was observed in the case of diammonium and triammonium organic functional groups. Also, for the same organoalkoxysilane/silica molar ratio, the adsorption capacity increased markedly with the increase of the number of protonated amines in the functional groups. Therefore, maximum adsorption capacities of 1.07, 1.70 and 2.46 mmol H(2)PO(4)(-)/g adsorbent were obtained using mono-, di- and tri-ammonium-functionalized SBA-15, respectively.

摘要

研究了单价磷酸盐阴离子从水溶液中在单、二和三铵官能化介孔 SBA-15 硅上的吸附。该吸附剂是通过后合成接枝法制备的,使用 3-氨丙基三甲氧基硅烷(N-硅烷)、[1-(2-氨基乙基)-3-氨丙基]三甲氧基硅烷(NN-硅烷)和 1-[3-(三甲氧基硅基)-丙基]-二乙三胺(NNN-硅烷),然后在 HCl 溶液中酸化,将附着的表面氨基转化为带正电荷的铵部分。氨基在 SBA-15 表面上的负载量为有机烷氧基硅烷/二氧化硅摩尔比从 5%变化到 40%。吸附实验在室温下分批进行。结果表明,无论官能团的性质如何,吸附容量都随着 SBA-15 吸附剂上官能团浓度的增加而增加。在单铵官能团的情况下,当有机烷氧基硅烷/二氧化硅摩尔比从 5%变化到 40%时,吸附容量从 0.64mmol H(2)PO(4)(-)增加到 1.07mmol H(2)PO(4)(-)。在二铵和三铵有机官能团的情况下也观察到了类似的趋势。此外,对于相同的有机烷氧基硅烷/二氧化硅摩尔比,随着官能团中质子化胺的数量增加,吸附容量显著增加。因此,使用单、二和三铵官能化 SBA-15 分别获得了 1.07mmol H(2)PO(4)(-)、1.70mmol H(2)PO(4)(-)和 2.46mmol H(2)PO(4)(-)的最大吸附容量。

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