Universidade Federal do Paraná, Departamento de Química, Laboratório de Bioinorgânica e Catálise e, CP 19081, CEP 81531-980, Curitiba, Paraná, Brazil.
J Colloid Interface Sci. 2012 May 15;374(1):278-86. doi: 10.1016/j.jcis.2012.02.014. Epub 2012 Feb 17.
Raw kaolinite was modified with triethanolamine (TEA), in an attempt to create a new support for the immobilization of metalloporphyrins. Anionic metalloporphyrins containing Fe(3+) or Mn(3+) as metallic centers were immobilized on the prepared support, and the obtained solids were characterized by Fourier-transform infrared (FTIR) spectroscopy, X-ray powder diffraction (XRPD), thermal analysis (thermogravimetric and differential thermal analyses--TGA/DTA), and scanning electron microscopy (SEM). The solids were used in heterogeneous oxidation catalysis of cyclooctene and cyclohexane. The yields from the oxidation of cyclooctene depended on the amount of TEA and/or water present in the solids. Good reaction yields were obtained for the oxidation of cyclohexane, with selectivity for the alcohol. In one specific case, a possible co-catalytic activity was verified for TEA during the oxidation of cyclohexane.
高岭土经三乙醇胺(TEA)改性,试图为金属卟啉的固定化创造一种新的载体。将含 Fe(3+)或 Mn(3+)作为金属中心的阴离子金属卟啉固定在制备的载体上,并用傅里叶变换红外(FTIR)光谱、X 射线粉末衍射(XRPD)、热分析(热重和差热分析-TGA/DTA)和扫描电子显微镜(SEM)对得到的固体进行了表征。这些固体用于环辛烯和环己烷的非均相氧化催化。环辛烯氧化的产率取决于固体中存在的 TEA 和/或水的量。环己烷的氧化得到了很好的反应产率,且对醇具有选择性。在一个特定的情况下,在环己烷氧化过程中,TEA 的共催化活性得到了验证。