通过共沉淀法、离子交换法、焙烧还原法制备出单十二烷基磷酸根离子(DDP)柱撑层状复合金属氢氧化物(LDHs)复合物。XRD和FT-IR分析表明,DDP进入到LDHs层间形成柱撑复合物,但采用3种工艺制备的复合物超分子结构有明显的不同:以共沉淀法制备的柱撑复合物层间距为3.15 nm,DDP在LDH层间呈倾斜双层排列,焙烧还原和离子交换法制备的复合物层间距为3.89 nm,DDP在LDH层间呈垂直双层排列。离子交换法制备出的DDP柱撑LDHs复合物中由于LDHs层间存在较强的静电作用力而不能使碳酸根被完全置换出来。
Layered double hydroxides(LDHs)/ Lauryl alcohol phosphoric acid ester(DDP) pillared compounds were synthesized by three different methods of co-precipitation,ion-exchange and calcined-rehydration respectively.The supramolecular structures of pillared compounds were characterized by power X-ray diffraction and Fourier transformation infrared spectra.Results indicated that DDP could intercalated into the interlayer of LDHs by three methods,but the supramolecular structure of pillared compounds had significant difference:the interlayer space of compound obtained by co-precipitation method is 3.15 nm,which shown that DDP has declining double layers structure in the lnterlayer of LDH;for the ion-exchange and calcined-rehydration compounds,the interlayer spaces are 3.89 nm,which implied that DDP is upright double layers arrange in the lnterlayer of LDH.And for the ion-exchange pillared compound,there existed anion of carbonate in the interlayer,which was not completely replaced by the DDP due to the strong electrostatic force of interlayer of LDHs.