High-resolution solid-state magic-angle spinning nuclear magnetic resonance studies on the thermal decomposition of the layered antimony hydrogen phosphate, HSb(PO4)2•2H2O

被引:3
作者
Carlino, S
Hudson, MJ
Locke, WJ
机构
[1] Univ Reading, Dept Chem, Reading RG6 2AD, Berks, England
[2] Univ Oxford, Dept Phys, Nucl Phys Lab, Oxford OX2 3RH, England
关键词
high-resolution solid-state MAS NMR; layered antimony hydrogen phosphate; pyrophosphate;
D O I
10.1016/S0167-2738(97)00501-8
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The antimony hydrogen phosphate, HSb(PO4)(2) . 2H(2)O, was synthesised using an ion-exchange method from the crystalline KSb(PO4)(2) precursor. The synthesised H1SbP2 . 2H(2)O material was then studied using P-31 and H-1 Magic-angle Spinning Nuclear Magnetic Resonance (MAS NMR) techniques. MAS NMR indicated that the synthesised phosphate consisted of Q(3)-type phosphate tetrahedra (i.e.; PO4) which were protonated in all cases. This was thought to be caused by the dynamic equilibrium between the mobile interlayer water and the protons randomly attached to alternate phosphate groups as H-O-(PO3)-R groups in the structure. Simultaneous TG and DTA thermogravimetry revealed a constant mass loss up to a temperature of 600 degrees C in the TG curve and a series of well defined thermal events in the DTA curve. Scanning electron microscopy revealed that the KSb(PO4)(2) was formed by the so-called 'deck of cards' mechanism. This technique also revealed that the ion-exchange to HSb(PO4)(2) . 2H(2)O resulted in delamination of the phosphate. BET (N-2) analysis of the synthesised material suggested a surface area of ca. 6.8 m(2) g(-1) and a range of pore sizes.
引用
收藏
页码:269 / 277
页数:9
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