کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1307779 1499155 2015 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Well-defined lanthanum ethylenediaminetetraacetates as the precursors of catalysts for the oxidative coupling of methane
ترجمه فارسی عنوان
اتیلندی دی آمین تترا اتانات لانتانیم تعریف شده به عنوان پیشرونده کاتالیزورها برای متصل کردن اکسیداتیو متان
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
چکیده انگلیسی


• Water-soluble MOF was constructed by lanthanide ethylenediaminetetraacetate with chloride.
• Lanthanum chloride, nitrate and sulfate were converted to pure LaOCl, La2O2CO3 and La2O2SO4 or their mixtures respectively.
• Thermal decomposition products demonstrate good catalytic performances for the oxidative coupling reaction of methane (OCM).

Water-soluble metal organic framework (MOF) complex [La5Cl2(edta)3(H2O)18]nCln·8nH2O (1) is converted to its nitrate or sulfate derivatives [La2(NO3)2(edta)(H2O)5]n·3nH2O (2), [La2(SO4)(edta)(H2O)3]n (3) (H4edta = C10H16N2O8, ethylenediaminetetraacetic acid). The three well-defined complexes are further calcinated for the preparations of pure lanthanum oxides LaOCl, La2O2CO3 and La2O2SO4 or their mixtures respectively. The oxides from 1 to 2 show good catalytic performances for the oxidative coupling reaction of methane (OCM). Their conversions of methane and the selectivities to C2 achieved 24.5%, 39.2% and 28.0%, 47.4% respectively at low temperature 550 °C, while the pure La2O2SO4 from 3 is not active at low temperature. The latter is contradict to the result by simple treatment of La2(SO4)3 reported previously.

Thermal products of [La5Cl2(edta)3(H2O)18]nCln·8nH2O (1) and [La2(NO3)2(edta)(H2O)5]n·3nH2O (2), demonstrate good catalytic performances for the oxidative coupling reaction of methane (OCM). While La2O2SO4 from [La2(SO4)(edta)(H2O)3]n (3) is not active at low temperature.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Inorganica Chimica Acta - Volume 434, 1 August 2015, Pages 221–229
نویسندگان
, , , , , , ,