کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
66134 48416 2012 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Single site anchored novel Cu(II) catalysts for selective liquid–gas phase O2 oxidation of n-alkanes
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Single site anchored novel Cu(II) catalysts for selective liquid–gas phase O2 oxidation of n-alkanes
چکیده انگلیسی

The pentacoordinate schiff-base trialkoxysilane Cu(II) complexes, i.e. Cu[Sal(PMeOSi)DPTA], (III-a) and Cu[Cl-Sal(PMeOSi)DPTA], (III-b) were synthesized and covalently anchored on SiO2 and Al2O3 matrixes as supported hybrid catalysts (i.e.III-a/SiO2 as Catal.-1, III-b/SiO2 as Catal.-2, III-a/Al2O3 as Catal.-3 and III-b/Al2O3 as Catal.-4). The characterization of supported Cu(II) complexes were performed with SEM-EDX, TGA, ICP, FT-IR and EPR analysis. Catalytic tests were conducted in the oxidation (O2) of n-alkanes under relatively mild conditions, in a batch rocking type reactor. Remarkable high catalytic TONs, from 1468 up to 2422, were observed. Catal.-2 provided the best overall yield, 25.2% with 92% selectivity for n-hexane and 20.1% with 75% selectivity for n-heptane. A 20% improvement in the yields was obtained with PCA as co-catalyst. The impact of both C- and O- centred radical traps were also assessed in order to establish a radical mechanism.

Synthesis, characterization and immobilized novel pentacoordinate trialkoxysilane Cu(II) complexes: application in selective n-alkanes oxidation with molecular O2 under optimize reaction conditions.Figure optionsDownload high-quality image (183 K)Download as PowerPoint slideHighlights
► Al2O3 or SiO2 single site anchored Cu complexes as supported hybrid catalysts.
► These catalysts have tested for n-hexane and n-heptane oxidation with O2 in batch reactor.
► High catalytic TONs from 1468 to 2422 were achieved under optimized reaction condition.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular Catalysis A: Chemical - Volume 357, May 2012, Pages 125–132
نویسندگان
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