Thermal behavior of kaolinite-urea intercalation complex and molecular dynamics simulation for urea molecule orientation
文献类型：期刊论文
| 作者 | Liu, Qinfu1; Zhang, Shuai1; Cheng, Hongfei1; Wang, Ding1; Li, Xiaoguang1; Hou, Xinjuan2; Frost, Ray L.3 |
| 刊名 | JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY
 |
| 出版日期 | 2014-07-01 |
| 卷号 | 117期号:1页码:189-196 |
| 关键词 | Kaolinite Urea Intercalation Thermal behavior Molecular dynamics simulation |
| ISSN号 | 1388-6150 |
| 其他题名 | J. Therm. Anal. Calorim. |
| 中文摘要 | The thermal behavior of kaolinite-urea intercalation complex was investigated by thermogravimetry-differential scanning calorimetry (TG-DSC), X-ray diffraction (XRD), and fourier transform infrared spectroscopy (FTIR). In addition, the interaction mode of urea molecules intercalated into the kaolinite gallery was studied by means of molecular dynamics simulation. Three main mass losses were observed at 136 A degrees C, in the range of 210-270 A degrees C, and at 500 A degrees C in the TG-DSC curves, which were, respectively, attributed to (1) melting of the surface-adsorbed urea, (2) removal of the intercalated urea, and (3) dehydroxylation of the deintercalated kaolinite. The three DSC endothermic peaks at 218, 250, and 261 A degrees C were related to the successive removals of intercalated urea with three different distribution structures. Based on the angle between the dipole moment vector of urea and the basal surface of kaolinite, the three urea models could be described as follows: (1) Type A, the dipole moment vector is nearly parallel to the basal surface of kaolinite; (2) Type B, the dipole moment vector points to the silica tetrahedron with the angle between it and the basal surface of kaolinite ranging from 20A degrees to 40A degrees; and (3) Type C, the dipole moment vector is nearly perpendicular to the basal surface of kaolinite. The three distribution structures of urea molecules were validated by the results of the molecular dynamics simulation. Furthermore, the thermal behavior of the kaolinite-urea intercalation complex investigated by TG-DSC was also supported by FTIR and XRD analyses. |
| 英文摘要 | The thermal behavior of kaolinite-urea intercalation complex was investigated by thermogravimetry-differential scanning calorimetry (TG-DSC), X-ray diffraction (XRD), and fourier transform infrared spectroscopy (FTIR). In addition, the interaction mode of urea molecules intercalated into the kaolinite gallery was studied by means of molecular dynamics simulation. Three main mass losses were observed at 136 A degrees C, in the range of 210-270 A degrees C, and at 500 A degrees C in the TG-DSC curves, which were, respectively, attributed to (1) melting of the surface-adsorbed urea, (2) removal of the intercalated urea, and (3) dehydroxylation of the deintercalated kaolinite. The three DSC endothermic peaks at 218, 250, and 261 A degrees C were related to the successive removals of intercalated urea with three different distribution structures. Based on the angle between the dipole moment vector of urea and the basal surface of kaolinite, the three urea models could be described as follows: (1) Type A, the dipole moment vector is nearly parallel to the basal surface of kaolinite; (2) Type B, the dipole moment vector points to the silica tetrahedron with the angle between it and the basal surface of kaolinite ranging from 20A degrees to 40A degrees; and (3) Type C, the dipole moment vector is nearly perpendicular to the basal surface of kaolinite. The three distribution structures of urea molecules were validated by the results of the molecular dynamics simulation. Furthermore, the thermal behavior of the kaolinite-urea intercalation complex investigated by TG-DSC was also supported by FTIR and XRD analyses. |
| WOS标题词 | Science & Technology ; Physical Sciences |
| 类目[WOS] | Chemistry, Analytical ; Chemistry, Physical |
| 研究领域[WOS] | Chemistry |
| 关键词[WOS] | BASAL SURFACES ; ORDERED KAOLINITE ; URANYL ADSORPTION ; POTASSIUM ACETATE ; ORGANIC-COMPOUNDS ; FORCE-FIELD ; NANOCOMPOSITES ; HYDRAZINE ; DECOMPOSITION ; SPECTROSCOPY |
| 收录类别 | SCI |
| 原文出处 | |
| 语种 | 英语 |
| WOS记录号 | WOS:000338120100020 |
| 公开日期 | 2014-08-28 |
| 版本 | 出版稿 |
| 源URL | [http://ir.ipe.ac.cn/handle/122111/10940]  |
| 专题 | 过程工程研究所_研究所（批量导入） |
| 作者单位 | 1.China Univ Min & Technol, Sch Geosci & Surveying Engn, Beijing 100083, Peoples R China 2.Chinese Acad Sci, Inst Proc Engn, Beijing 100080, Peoples R China 3.Queensland Univ Technol, Sch Chem Phys & Mech Engn, Fac Sci & Engn, Brisbane, Qld 4001, Australia |
| 推荐引用方式 GB/T 7714 | Liu, Qinfu,Zhang, Shuai,Cheng, Hongfei,et al. Thermal behavior of kaolinite-urea intercalation complex and molecular dynamics simulation for urea molecule orientation[J]. JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY,2014,117(1):189-196. |
| APA | Liu, Qinfu.,Zhang, Shuai.,Cheng, Hongfei.,Wang, Ding.,Li, Xiaoguang.,...&Frost, Ray L..(2014).Thermal behavior of kaolinite-urea intercalation complex and molecular dynamics simulation for urea molecule orientation.JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY,117(1),189-196. |
| MLA | Liu, Qinfu,et al."Thermal behavior of kaolinite-urea intercalation complex and molecular dynamics simulation for urea molecule orientation".JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY 117.1(2014):189-196. |
入库方式： OAI收割
来源：过程工程研究所
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