کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
72506 49023 2015 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Liquid-assisted mechanochemical synthesis of an iron carboxylate Metal Organic Framework and its evaluation in diesel fuel desulfurization
ترجمه فارسی عنوان
سنتز مکانیکمی شیمیایی مایع مشتق شده از یک فلز کربوکسیلات فلزی و ارزیابی آن در سولفوریزاسیون سوخت دیزل
کلمات کلیدی
مایع مایع کمک، چارچوب فلزی-ارگانیک، سولفوریزاسیون، 4،6-دی متیلید بنزوتیوفن
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
چکیده انگلیسی


• Iron (III) carboxylate MOF is obtained by mechanochemical approach.
• Liquid-assisted mechanochemical synthesis yields the MOF in 1 h at RT and atmospheric pressure.
• Crystallinity and textural features are superior to those of a commercial sample.
• 4,6-Dimetyldibenzothiophene is adsorbed to a higher extent on the ball-milled sample.

An iron (III) carboxylate Metal Organic Framework isostructural with MIL-100(Fe) was synthesized through a mechanochemical route. The material, rapidly obtained by liquid-assisted grinding at room temperature, was characterized by X-ray powder diffraction, infrared spectroscopy, scanning electron microscopy, thermal gravimetry, nitrogen physisorption and adsorption microcalorimetry of ammonia. For comparison, the features of a commercial iron trimesate produced via electrochemical route were investigated as well. The ball-milled sample showed better crystallinity, associated with good thermal stability, higher surface area and pore volume. The adsorption performance of both the ball-milled and commercial samples for the ambient-temperature removal of 4,6-dimethyldibenzothiophene (4,6-DMDBT) from 4,6-DMDBT)/n-heptane solutions simulating a diesel fuel was also investigated. The maximum adsorption capacity for the ball-milled sample resulted twice as big as that for the commercial one. An interpretation of the different adsorption behavior is proposed.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Microporous and Mesoporous Materials - Volume 213, 1 September 2015, Pages 14–21
نویسندگان
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