lead caprate;lead(II) neodecanoate;lead(II) decanoate;decanoic acid ; lead caprinate;Decansaeure; Blei(II)-Verbindung;Decansaeure; Bleicaprinat;Decanoic acid, lead salt;decanoate;lead(2+)
lead decanoate 以
neat (no solvent) 为溶剂,
生成 lead(II) oxide
参考文献:
名称:
Investigation of the pyrolysis of lead zirconate titanate gels with coupled differential thermal analysis, thermogravimetry and infrared spectroscopy
摘要:
The pyrolysis of organic components in the sol-gel preparation of lead zirconate titanate (PZT) from lead acetate and zirconium and titanium propanolate in methoxyethanol is studied with simultaneous differential thermal analysis, thermogravimetry and infrared spectroscopy. The first pyrolysis step of the dried PPT gel, yielding acetone and CO2 similar to the pyrolysis of lead acetate, indicates that most of the acetate groups are bonded to Pb2+ In the second step, the remaining organic components are oxidized to CO2 and H2O. The formation of undesired carbon residues during pyrolysis from unhydrolysed alkoxide groups and acetate groups bonded to Zr4+ and Ti4+ can be prevented by steam treatment of the dried gels. Activation energies for the different pyrolysis steps of lead, zirconium and titanyl acetate, lead decanoate and PZT gels are given. (C) 1998 Kluwer Academic Publishers.
Lead(<scp>ii</scp>) soaps: crystal structures, polymorphism, and solid and liquid mesophases
作者:F. J. Martínez-Casado、M. Ramos-Riesco、J. A. Rodríguez-Cheda、M. I. Redondo-Yélamos、L. Garrido、A. Fernández-Martínez、J. García-Barriocanal、I. da Silva、M. Durán-Olivencia、A. Poulain
DOI:10.1039/c7cp02351k
日期:——
phases and mesophases. The crystal structures at room temperature of all of the members of the series are now solved, showing the existence of two polymorphic forms in the room temperature crystal phase, different to short and long-chain members. Only nonanoate and decanoate present both forms, and this polymorphism is proven to be monotropic. At higher temperature, these compounds present a solid mesophase
作者:Joseph V. Mantese、Norman W. Schubring、Adolph L. Micheli、Margarita P. Thompson、Ratna Naik、Gregory W. Auner、I. Burc Misirlioglu、S. Pamir Alpay
DOI:10.1063/1.1498506
日期:2002.8.5
Polarization-gradedferroelectrics and their electrically active embodiments, graded ferroelectric devices and transpacitors, have been formed from a variety of material systems, both by grading the composition of the ferroelectric and by imposing temperature gradients normal to the electrode surfaces. In this letter, we show how these same devices can be formed from homogeneous ferroelectric films
Coordination geometry of lead carboxylates – spectroscopic and crystallographic evidence
作者:Jaclyn Catalano、Anna Murphy、Yao Yao、Glenn P. A. Yap、Nicholas Zumbulyadis、Silvia A. Centeno、Cecil Dybowski
DOI:10.1039/c4dt03075c
日期:——
Spectroscopic and crystallographic data show lead carboxylate coordination is chain length dependent, shorter-chains (C6–C8) are hemidirected and longer-chains (C9–C18) are holodirected.
Investigation of the pyrolysis of lead zirconate titanate gels with coupled differential thermal analysis, thermogravimetry and infrared spectroscopy
作者:R. MERKLE、R. MERKLE
DOI:10.1023/a:1004476613569
日期:1998.9
The pyrolysis of organic components in the sol-gel preparation of lead zirconate titanate (PZT) from lead acetate and zirconium and titanium propanolate in methoxyethanol is studied with simultaneous differential thermal analysis, thermogravimetry and infrared spectroscopy. The first pyrolysis step of the dried PPT gel, yielding acetone and CO2 similar to the pyrolysis of lead acetate, indicates that most of the acetate groups are bonded to Pb2+ In the second step, the remaining organic components are oxidized to CO2 and H2O. The formation of undesired carbon residues during pyrolysis from unhydrolysed alkoxide groups and acetate groups bonded to Zr4+ and Ti4+ can be prevented by steam treatment of the dried gels. Activation energies for the different pyrolysis steps of lead, zirconium and titanyl acetate, lead decanoate and PZT gels are given. (C) 1998 Kluwer Academic Publishers.