Tripodal Ligand-Stabilized Layered Double Hydroxide Nanoparticles with Highly Exchangeable CO32–

羟甲基 氢氧化物 化学 配体(生物化学) 纳米颗粒 无机化学 粒径 水溶液 核化学 立体化学 物理化学 材料科学 纳米技术 生物化学 受体
作者
Yoshiyuki Kuroda,Y. Miyamoto,Mitsuhiro Hibino,Kazuya Yamaguchi,Noritaka Mizuno
出处
期刊:Chemistry of Materials [American Chemical Society]
卷期号:25 (11): 2291-2296 被引量:114
标识
DOI:10.1021/cm400846k
摘要

Layered double hydroxide nanoparticles (LDHNPs) with exceptionally small particle sizes are synthesized using a tripodal ligand of tris(hydroxymethyl)aminomethane (THAM). For example, a LDHNP with the average size of 9.7 nm (denoted as LDH(10 nm), containing CO32– in the interlayer), can be synthesized using a 2.0 M THAM solution. The 13C CP/MAS NMR and FTIR analyses show that THAM is ligated to the layer as an alkoxide species. The average particle size of LDH synthesized using l-lysine (buffering base) instead of THAM is larger (47.9 nm) than that of LDH(10 nm). Therefore, the size reduction is possibly explained by the specific interaction of THAM with the layer via its multiple coordination. In addition, it is confirmed by the 13C CP/MAS NMR analysis that LDH(10 nm) possesses CO32– species weakly interacting with the layers. LDHNPs, in particular, as-synthesized LDH(10 nm) (denoted as LDH(10 nm)-as, containing CO32– and Cl– in the interlayer), possesses the extremely high anion exchange abilities, and almost all anions in LDH(10 nm)-as are potentially exchangeable with NO3–, even under ambient (CO2-existing) conditions. Furthermore, LDH(10 nm)-as can act as an efficient reusable scavenger for harmful oxyanions and remove arsenic, selenium, and boron from their dilute aqueous solutions under ambient conditions.
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